Plant transcriptional regulators

ABSTRACT

The invention relates to plant transcription factor polypeptides, polynucleotides that encode them, homologs from a variety of plant species, and methods of using the polynucleotides and polypeptides to produce transgenic plants having improved tolerance to drought, shade, and low nitrogen conditions, as compared to wild-type or reference plants.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a division of U.S. patent application Ser. No.15/821,061, filed Nov. 22, 2017 (now U.S. Pat. No. 10,266,575) whichapplication is a division of U.S. patent application Ser. No.14/229,574, filed Mar. 28, 2014 (now U.S. Pat. No. 9,856,297) whichapplication is a division of U.S. patent application Ser. No.14/167,768, filed Jan. 29, 2014 (abandoned) which application is adivision of U.S. patent application Ser. No. 12/705,845, filed Feb. 15,2010 (now U.S. Pat. No. 8,686,226). application Ser. No. 12/705,845 isalso a continuation-in-part of U.S. patent application Ser. No.11/435,388, filed May 15, 2006 (now U.S. Pat. No. 7,663,025), whichapplication is a continuation-in-part of PCT patent application no.PCT/US2004/037584, filed Nov. 12, 2004 (expired). PCT/US2004/037584 is acontinuation-in-part of U.S. patent application Ser. No. 10/714,887,filed Nov. 13, 2003 (abandoned). PCT/US2004/037584 claims the benefit ofU.S. provisional patent application No. 60/542,928, filed Feb. 5, 2004(expired) and PCT/US2004/037584 also claims the benefit of U.S.provisional patent application No. 60/527,658, filed Dec. 5, 2003(expired). application Ser. No. 12/705,845 is also acontinuation-in-part of U.S. patent application Ser. No. 10/714,887,filed Nov. 13, 2003 (abandoned), which application is acontinuation-in-part of U.S. patent application Ser. No. 10/412,699,filed Apr. 10, 2003 (now U.S. Pat. No. 7,345,217). application Ser. No.10/714,887 is also a continuation-in-part of U.S. patent applicationSer. No. 10/456,882, filed Jun. 6, 2003 (abandoned). application Ser.No. 10/714,887 is also a continuation-in-part of U.S. patent applicationSer. No. 10/374,780, filed Feb. 25, 2003 (now U.S. Pat. No. 7,511,190).application Ser. No. 10/714,887 is also a continuation-in-part of U.S.patent application Ser. No. 10/666,642, filed Sep. 18, 2003 (now U.S.Pat. No. 7,196,245), which application claims the benefit of U.S.provisional patent application No. 60/434,166, filed Dec. 17, 2002(expired). application Ser. No. 10/666,642 also claims the benefit ofU.S. provisional patent application No. 60/411,837, filed Sep. 18, 2002(expired). application Ser. No. 10/666,642 also claims the benefit ofU.S. provisional patent application No. 60/465,809, filed Apr. 24, 2003(expired). application Ser. No. 12/705,845 is also acontinuation-in-part of U.S. patent application Ser. No. 11/981,576,filed Oct. 30, 2007 (now U.S. Pat. No. 7,888,558), and U.S. patentapplication Ser. No. 11/981,576 is a continuation-in-part of U.S. patentapplication Ser. No. 10/456,882, filed Jun. 6, 2003 (abandoned). All ofthese applications are hereby incorporated by reference in theirentirety.

JOINT RESEARCH AGREEMENT

The claimed invention, in the field of functional genomics and thecharacterization of plant genes for the improvement of plants, was madeby or on behalf of Mendel Biotechnology, Inc. and Monsanto Company as aresult of activities undertaken within the scope of a joint researchagreement in effect on or before the date the claimed invention wasmade.

FIELD OF THE INVENTION

The present invention relates to compositions and methods for modifyingthe phenotype of a plant, including altered carbon/nitrogen balancesensing, improved nitrogen uptake or assimilation efficiency, improvedgrowth or survival of plants under conditions of nitrogen limitation,increased tolerance to drought or other abiotic stress, and/or increasedtolerance to shade.

BACKGROUND OF THE INVENTION

A plant's traits may be controlled through a number of cellularprocesses. One important way to manipulate that control is throughtranscription factors—proteins that influence the expression of aparticular gene or sets of genes. Because transcription factors are keycontrolling elements of biological pathways, altering the expressionlevels of one or more transcription factors can change entire biologicalpathways in an organism. Strategies for manipulating a plant'sbiochemical, developmental, or phenotypic characteristics by altering atranscription factor expression can result in plants and crops with newand/or improved commercially valuable properties, including traits thatimprove yield or survival and yield during periods of abiotic stress,improve shade tolerance, or alter a plant's sensing of itscarbon/nitrogen balance.

We have identified numerous polynucleotides encoding transcriptionfactors, functionally related sequences listed in the Sequence Listing,and structurally and functionally similar sequences, developed numeroustransgenic plants using these polynucleotides, and analyzed the plantsfor their tolerance to shade, drought stress, and alteredcarbon-nitrogen balance (C/N) sensing. In so doing, we have identifiedimportant polynucleotide and polypeptide sequences for producingcommercially valuable plants and crops as well as the methods for makingthem and using them. The present invention thus relates to methods andcompositions for producing transgenic plants with improved tolerance todrought and other abiotic stresses, with altered C/N sensing, and/orwith improved tolerance to shade. This provides significant value inthat the plants may thrive in hostile environments where low nutrient,light, or water availability limits or prevents growth of non-transgenicplants. Other aspects and embodiments of the invention are describedbelow and can be derived from the teachings of this disclosure as awhole.

SUMMARY OF THE INVENTION

The present method is directed to recombinant polynucleotides thatconfer abiotic stress tolerance in plants when the expression of any ofthese recombinant polynucleotides is altered (e.g., by overexpression).Related sequences that are encompassed by the invention includenucleotide sequences that hybridize to the complement of the sequencesof the invention under stringent conditions.

Related sequences that are also encompassed by the invention includepolypeptide sequences within a given clade or subclade, that is,sequences that are evolutionarily, functionally and structurallyrelated. The invention also pertains to a transgenic plant thatcomprises a recombinant polynucleotide that encodes a polypeptide thatregulates transcription.

The invention also includes a transgenic plant that overexpresses arecombinant polynucleotide comprising a nucleotide sequence thathybridizes to the complement of any polynucleotide of the inventionunder stringent conditions. This transgenic plant has increased drought,low nitrogen and/or shade tolerance as compared to a wild-type ornon-transformed plant of the same species that does not overexpress apolypeptide encoded by the recombinant polynucleotide.

The invention also encompasses a method for producing a transgenic planthaving increased tolerance to drought, low nitrogen, and/or shade. Thesemethod steps include first providing an expression vector that containsa nucleotide sequence that hybridizes to the complement of apolynucleotide of the invention under stringent hybridizationconditions. The expression vector is then introduced into a plant cell,the plant cell is cultured, from which a plant is generated. Due to thepresence of the expression vector in the plant, the polypeptide encodedby the nucleotide sequence is overexpressed. This polypeptide has theproperty of regulating drought, low nitrogen, or shade tolerance in aplant, compared to a control plant that does not overexpress thepolypeptide. After the drought, low nitrogen, or shade-toleranttransgenic plant is produced, it may be identified by comparing it withone or more non-transformed plants that do not overexpress thepolypeptide. These method steps may further include selfing or crossingthe abiotic stress-tolerant plant with itself or another plant,respectively, to produce seed. “Selfing” refers to self-pollinating, orusing pollen from one plant to fertilize the same plant or another plantin the same line, whereas “crossing” generally refers to crosspollination with plant from a different line, such as a non-transformedor wild-type plant, or another transformed plant from a differenttransgenic line of plants. Crossing provides the advantage of being ableto produce new varieties. The resulting seed may then be used to grow aprogeny plant that is transgenic and has increased tolerance to abioticstress.

The invention is also directed to a method for increasing a plant'stolerance to drought, low nitrogen, or shade. This method includes firstproviding a vector that comprises (i) regulatory elements effective incontrolling expression of a polynucleotide sequence in a target plant,where the regulatory elements flank the polynucleotide sequence; and(ii) the polynucleotide sequence itself, which encodes a polypeptidethat has the ability to regulate drought, low nitrogen, or shadetolerance in a plant, as compared to a control plant of the same speciesthat does not overexpress the polypeptide. The plant is transformed withthe vector in order to generate a transformed plant with increasedtolerance to drought, low nitrogen, or shade.

BRIEF DESCRIPTION OF THE SEQUENCE LISTING AND FIGURES

The Sequence Listing provides exemplary polynucleotide and polypeptidesequences of the invention. The traits associated with the use of thesequences are included in the Examples.

INCORPORATION OF THE SEQUENCE LISTING

The copy of the Sequence Listing, being submitted electronically withthis patent application, provided under 37 CFR § 1.821-1.825, is aread-only memory computer-readable file in ASCII text format. TheSequence Listing is named“MDBT008USD2-sequence_listing_replacement.txt”, the electronic file ofthe Sequence Listing was created on Jul. 27, 2015, and is 2,500,656bytes in size (or 2,500 kilobytes in size as measured in MS-WINDOWS).The Sequence Listing is herein incorporated by reference in itsentirety.

FIGURES

For figures presenting one or more sequences, the SEQ ID NO: of thesequence(s) is/are provided in parentheses.

FIG. 1 shows a conservative estimate of phylogenetic relationships amongthe orders of flowering plants (modified from Angiosperm Phylogeny Group(1998) Ann. Missouri Bot. Gard. 84: 1-49). Those plants with a singlecotyledon (monocots) are a monophyletic clade nested within at least twomajor lineages of dicots; the eudicots are further divided into rosidsand asterids. Arabidopsis is a rosid eudicot classified within the orderBrassicales; rice is a member of the monocot order Poales. FIG. 1 wasadapted from Daly et al. (2001) Plant Physiol. 127: 1328-1333.

FIG. 2 shows a phylogenic dendogram depicting phylogenetic relationshipsof higher plant taxa, including clades containing tomato andArabidopsis; adapted from Ku et al. (2000) Proc. Natl. Acad. Sci. 97:9121-9126; and Chase et al. (1993) Ann. Missouri Bot. Gard. 80: 528-580.

FIG. 3 is a multiple amino acid sequence alignment of subsequence withinthe AP2 domain of G47, G2133 and their orthologs. The first column showsthe sequence name followed by the SEQ ID No. in parentheses. Cladeorthologs and paralogs are indicated by the black bar on the left sideof the figure. Of the sequences examined to date, two valine residueswere found that are present in members of the G47 clade but not outsideof the clade (arrows). Residues that may be used to identify a G47 clademember are indicated by the residues shown in the boxes in FIG. 3

FIG. 4 illustrates the relationship of G47 and related sequences in thisphylogenetic tree of the G47 Glade and similar sequences. The treebuilding method used was “Neighbor Joining” with “SystematicTie-Breaking” and Bootstrapping with 1000 replicates (Uncorrected (“p”),with gaps distributed proportionally). Full-length polypeptides wereused to build the phylogeny as defined in FIG. 4. The members of theclade shown within the box are predicted to contain functional homologsof G47. Abbreviations: At Arabidopsis thaliana; Os Oryza sativa; Zm Zeamays; Gm Glycine max; Mt Medicago truncatula; Br Brassica rapa; BoBrassica oleracea; Ze: Zinnia elegans.

FIGS. 5A and 5B compare the recovery from a drought treatment ofwild-type controls and two lines of Arabidopsis plants overexpressingG2133, a paralog of G47. FIGS. 5A and 5B show two 35S::G2133 lines ofplants (one line in each figure) in the pot on the left of each figureand control plants on the right of each figure. Each pot containedseveral plants grown under 24 hours light. All were deprived of waterfor eight days, and are shown after re-watering. All of the plants ofthe G2133 overexpressor lines recovered, and all of the control plantswere either dead or severely and adversely affected by the droughttreatment.

FIGS. 6A-6C compare a number of homeodomains from thezinc-finger-homeodomain-type (ZF-HD) proteins related to G2999. Thefirst column shows the sequence name followed by the SEQ ID No. inparentheses. _Homeodomains from the ZF-HD type proteins are distinctfrom classical types of homeodomains and lie on the distinct branch ofthe tree shown in FIG. 7. The relationships established from this typeof alignment of homeodomains were used to generate the phylogenetic treeshown in FIGS. 7 and 8. Residues that may be used to identify the G2999clade are shown in boxes in FIGS. 6A and 6B.

FIG. 7 illustrates the relationship of G2999 and related sequences inthis phylogenetic tree of the G2999 clade and similar sequencescomprising ZF-HD-type proteins. The tree building method used was“Neighbor Joining” with “Systematic Tie-Breaking” and Bootstrapping with1000 replicates (Uncorrected (“p”), with gaps distributedproportionally. All of the sequences shown are members of the clade andare predicted to be functional homologs of G2999. Abbreviations: AtArabidopsis thaliana; Os (jap) Oryza sativa (japonica cultivar group);Os (ind) Oryza sativa (indica cultivar group); Zm Zea mays; Lj Lotuscorniculatus var. japonicus; Bn Brassica napus; Fb Flaveria bidentis.

FIG. 8 is a phylogenetic tree (neighbor-joining, 1000 bootstraps)highlighting the relational differences between the ZF-HD type proteinsand the “classical” homeodomain (HD) proteins. The homeodomains fromZF-HD type proteins lie on a distinct branch of the tree compared toclassical types of homeodomains (arrow).

FIGS. 9A-9L represent a multiple amino acid sequence alignment of G1792orthologs and paralogs. The first column shows the sequence namefollowed by the SEQ ID No. in parentheses. Clade orthologs and paralogsare indicated by the black bar on the left side of the figure. Conservedregions of identity are boxed and bolded while conserved sequences ofsimilarity are boxed with no bolding. The AP2 conserved domains spanalignment coordinates 196-254. The S conserved domain spans alignmentcoordinates of 301-304. The EDLL conserved domain spans the alignmentcoordinates of 393-406 (also see FIG. 10). Abbreviations: At Arabidopsisthaliana; Os Oryza sativa; Zm Zea mays; Ta Triticum aestivum; Gm Glycinemax; Mt Medicago truncatula.

FIG. 10 shows a novel conserved domain for the G1792 clade, hereinreferred to as the “EDLL domain”. The first column shows the sequencename followed by the SEQ ID No. in parentheses. All clade memberscontain a glutamic acid residue at position 3, an aspartic acid residueat position 8, and a leucine residue at positions 12 and 16.Abbreviations: At Arabidopsis thaliana; Os Oryza sativa; Zm Zea mays; TaTriticum aestivum; Gm Glycine max; Mt Medicago truncatula.

FIG. 11 illustrates the relationship of G1792 and related sequences inthis phylogenetic tree of the G1792 clade of transcription factors. Thetree building method used was “Neighbor Joining” with “SystematicTie-Breaking” and Bootstrapping with 1000 replicates. Only conserveddomains were used to build the phylogeny as defined in FIG. 11. Themembers of the G1792 clade are shown within the box. The sequenceswithin the G1792 clade descend from a common ancestral node (arrow).

FIG. 12 shows an alignment of G3086, orthologs, and paralogsubsequences. The first column shows the sequence name followed by theSEQ ID No. in parentheses. The G3086 clade is indicated by the black baron the left side of the figure. Residues that may be used to identifyclade members appear in boxes.

FIG. 13 is a phylogenetic tree of the G3086 clade, including G3086 andits paralogs and orthologs. Full length, predicted protein sequenceswere used to construct a pairwise comparison, bootstrapped (1000replicates) neighbor-joining tree, consensus view. Sequences within theG3086 clade are located within the box. The sequences within the G3086clade descend from a common ancestral node (arrow). Abbreviations: AtArabidopsis thaliana; Os Oryza sativa; Zm Zea mays; Gm Glycine max.

FIGS. 14A-14R show a multiple amino acid sequence alignment of G922orthologs and paralogs. The first column shows the sequence namefollowed by the SEQ ID No. in parentheses. Clade orthologs and paralogsare indicated by black bar on the left side of the figure. Residues thatappear in boldface represent an acidic, ser/pro-rich domain that isunique to the G922 clade. Abbreviations: At Arabidopsis thaliana; OsOryza sativa; Zm Zea mays; Ta Triticum aestivum; Gm Glycine max; LeLycopersicon esculentum; Ps Pisum sativum.

FIG. 15 is a phylogenetic tree of the G922 paralogs and orthologs. Fulllength, predicted protein sequences were used to construct a pairwisecomparison, bootstrapped (1000 replicates) neighbor-joining tree,consensus view. Sequences within the G922 clade are located within thebox.

FIG. 16 is a sequence alignment of predicted protein subsequences withinthe WRKY domain from G1274 paralogs and orthologs. The first columnshows the sequence name followed by the SEQ ID No. in parentheses. Thesequences within the G1274 clade are indicated by the black bar to theleft of the sequences. Amino acid residues within the WRKY domain thatdistinguish the G1274 clade sequences, and are putatively responsiblefor conserved functionality, are indicated within the boxes.

FIG. 17 represents a phylogenetic tree for the G1274 paralogs andorthologs. Full length, predicted protein sequences were used toconstruct a bootstrapped (1000 replicates) neighbor-joining tree. Gapsand missing data were handled using pairwise deletion and the distancemethod used was p-distance. Sequences within the G1274 clade appearwithin the box.

FIGS. 18A-18BB show a multiple sequence alignment of predicted proteinsequences from G2053, and its paralogs and orthologs. The first columnshows the sequence name followed by the SEQ ID No. in parentheses. Thesequences within the G2053 clade are indicated by the black bar to theleft of the alignment. The amino acid residues in boldface are consensusresidues, and those within the boxes represent conserved, similarresidues. Sequences without a species identifier were found inArabidopsis.

FIG. 19 is a phylogenetic tree for the G2053 paralogs and orthologs.Full length, predicted protein sequences were used to construct abootstrapped (1000 replicates) neighbor-joining tree. Gaps and missingdata were handled using pairwise deletion and the distance method usedwas p-distance. Sequences within the G2053 Glade appear within the box.

FIGS. 20A and 20B show the conserved domains making up the DNA bindingdomains of G682-like proteins from Arabidopsis, soybean, rice, and corn.The first column shows the sequence name followed by the SEQ ID No. inparentheses. G682 and its paralogs and orthologs are almost entirelycomposed of a single repeat MYB-related DNA binding domain that ishighly conserved across plant species. The polypeptide sequences thatare representatives of the G682 subclade are denoted by the vertical barto the left of the subsequences. The residues in the boxes in FIG. 20Bmay be used to identify G682 subclade members. The residues indicated bythe arrows and in the boxes in FIG. 20B have not been found atcorresponding positions in sequences outside of the G682 subclade. Priorto this disclosure, no function such as those presented in Example VIIIhas been identified for any of the non-Arabidopsis MYB-related sequencesin the G682 subclade.

FIG. 21 illustrates the relationship of G682 and related sequences inthis phylogenetic tree of the G682 subclade and similar sequences. Thisphylogenetic tree of defined conserved domains of G682 and relatedpolypeptides was constructed with ClustalW (CLUSTAL W Multiple SequenceAlignment Program version 1.83, 2003) and MEGA2(http://www.megasoftware.net) software. ClustalW multiple alignmentparameters were as follows:

Gap Opening Penalty: 10.00

Gap Extension Penalty: 0.20

Delay divergent sequences: 30%

DNA Transitions Weight: 0.50

Protein weight matrix: Gonnet series

DNA weight matrix: IUB

Use negative matrix: OFF

A FastA formatted alignment was then used to generate a phylogenetictree in MEGA2 using the neighbor joining algorithm and a p-distancemodel. A test of phylogeny was done via bootstrap with 100 replicationsand Random Speed set to default. Cut off values of the bootstrap treewere set to 50%. The G682 subclade of MYB-related transcription factors,a group of structurally and functionally related sequences that derivefrom a single ancestral node (arrow), appears within the box in FIG. 21.Most of the members of the subclade within the box have been shown toconfer abiotic stress tolerance and/or altered C/N sensing when thepolypeptides are overexpressed (see Table 13).

FIG. 22 is a graph representing light quality (percent transmission vs.wavelength) in the controlled environment plant growth chamber used forthe shade avoidance studies. Because shading is detected usingphytochrome to sense the R:FR ratio in light, we can mimic the effect ofshading by using a filter designed to prevent only the transmission ofred wavelengths. To determine whether the mechanisms used to senseshading are altered, we exploit the observation that seedlings ofwild-type plants grown under light deficient in red wavelengths haveextended hypocotyls, indicating a shade avoidance phenotype. Plantsoverexpressing genes which produce short hypocotyls under theseconditions, and exhibit a shade tolerance phenotype, would be candidatesfor further examination in more rigorous studies (e.g., by looking atcomponents such as yield under high densities in greenhouse studies).For the data seen in FIG. 22, a small piece of the filter was removedand used to determine the percent transmission with a Beckman DU-650spectrophotometer. This filter effectively removed the red region of thevisible spectrum yet allowed far-red and blue to pass through.

FIG. 23 shows the results of an experiment with 35S::G634 plants versuswild type. Individual seedlings were compared after being grown underlight deficient in red wavelengths (b/FR) and white light (w). The G634overexpressors did not exhibit a shade avoidance phenotype, as indicatedby their short hypocotyls produced under these conditions.

DETAILED DESCRIPTION OF THE SPECIFIC EMBODIMENTS

The data presented herein represent the results of a screen of atranscription factor collection to identify genes that can be applied toreduce yield losses that arise from low nutrient, drought-relatedstress, and/or shade avoidance responses.

We have identified numerous transcription factor genes that conferimproved drought-tolerance relative to wild type plants when theirexpression is altered, such as by overexpression or knocking-out of thegene in transgenic plants. Thus, the present invention is directed inpart to recombinant polynucleotides that confer drought-related stresstolerance in plants when the expression of recombinant polynucleotidesof the invention is altered (e.g., by overexpression). In the presentstudies, soil-based assays were performed in which transgenic plants arefirst deprived of water, evaluated by comparison to control plants,rewatered, and their recovery also evaluated by comparison to controlplants similarly treated.

We have also identified numerous transcription factor genes that conferaltered C/N sensing in transgenic Arabidopsis plants. These experimentswere carried out in two phases. A primary screen was done on seed lotscomprised of seed mixed together from each of two or three independentprimary transformants, or on a homozygous population in the case of theknockout lines. Any lot which showed a C/N sensing phenotype wassubjected to a repeat experiment. Transgenic lines that exhibited analtered C/N sensing phenotype in repeat experiments, as compared tocontrol plants, are shown in the tables and Sequence Listing.

A secondary screen was then conducted in which either two or threeindividual overexpression lines (or a different homozygous seed lot, inthe case of knockout lines) were retested in the assay. The individualtransgenic lines that showed prominent phenotypes in the second roundassay were given an “A” priority ranking. The set of sequences assigneda “B” priority ranking in the results table have yet to be confirmed inthe secondary screen or did not show a prominent phenotype.

We have also identified numerous transcription factor genes that confershade tolerance in transgenic Arabidopsis plants. The principle behindthe experiment was as follows: angiosperm plants have evolved mechanismsto compete with neighboring vegetation for light. When incident light isfiltered or reflected by adjacent plants, the red wavelengths of thespectrum are removed, resulting in a fall in the ratio of red to far redlight that the plant perceives. These changes are detected via thephytochrome photoreceptors and result in extension type growth andaccelerated flowering. Such responses reduce the resources available forstorage and reproduction, which in turn results in poor fruit and seeddevelopment and reduced yield. Given that shade avoidance responses areoften initiated in crops at planting densities where light availabilityis not a limiting growth factor, genes that suppress such effects wouldoffer yield savings.

In the experiments presented herein, overexpression and mutantArabidopsis lines for a transcription factor collection were grown underlight that was deficient in red wavelengths, and was thereforeequivalent to light shaded by vegetation. Transcription factors wereidentified that conferred shade tolerance and prevented the elongatedgrowth that was produced in wild-type controls under such conditions.

The present invention relates in part to polynucleotides andpolypeptides, for example, for modifying phenotypes of plants,particularly those associated with altered C/N sensing, and improveddrought stress and shade tolerance. Throughout this disclosure, variousinformation sources are referred to and/or are specificallyincorporated. The information sources include scientific journalarticles, patent documents, textbooks, and World Wide Webbrowser-inactive page addresses. While the reference to theseinformation sources clearly indicates that they can be used by one ofskill in the art, each and every one of the information sources citedherein are specifically incorporated in their entirety, whether or not aspecific mention of “incorporation by reference” is noted. The contentsand teachings of each and every one of the information sources can berelied on and used to make and use embodiments of the invention.

As used herein and in the appended claims, the singular forms “a,” “an,”and “the” include plural reference unless the context clearly dictatesotherwise. Thus, for example, a reference to “a plant” includes aplurality of such plants, and a reference to “a stress” is a referenceto one or more stresses and equivalents thereof known to those skilledin the art, and so forth.

Definitions

“Nucleic acid molecule” refers to an oligonucleotide, polynucleotide orany fragment thereof. It may be DNA or RNA of genomic or syntheticorigin, double-stranded or single-stranded, and combined withcarbohydrate, lipids, protein, or other materials to perform aparticular activity such as transformation or form a useful compositionsuch as a peptide nucleic acid (PNA).

“Polynucleotide” is a nucleic acid molecule comprising a plurality ofpolymerized nucleotides, for example, at least about 15 or moreconsecutive polymerized nucleotides. A polynucleotide may be a nucleicacid, oligonucleotide, nucleotide, or any fragment thereof. In manyinstances, a polynucleotide comprises a nucleotide sequence encoding apolypeptide (or protein) or a domain or fragment thereof. Additionally,the polynucleotide may comprise a promoter, an intron, an enhancerregion, a polyadenylation site, a translation initiation site, 5′ or 3′untranslated regions, a reporter gene, a selectable marker, or the like.The polynucleotide can be single-stranded or double-stranded DNA or RNA.The polynucleotide optionally comprises modified bases or a modifiedbackbone. The polynucleotide can be, for example, genomic DNA or RNA, atranscript (such as an mRNA), a cDNA, a PCR product, a cloned DNA, asynthetic DNA or RNA, or the like. The polynucleotide can be combinedwith carbohydrate, lipids, protein, or other materials to perform aparticular activity such as transformation or form a useful compositionsuch as a peptide nucleic acid (PNA). The polynucleotide can comprise asequence in either sense or antisense orientations. “Oligonucleotide” issubstantially equivalent to the terms amplimer, primer, oligomer,element, target, and probe and is preferably single-stranded.

“Gene” or “gene sequence” refers to the partial or complete codingsequence of a gene, its complement, and its 5′ or 3′ untranslatedregions. A gene is also a functional unit of inheritance, and inphysical terms is a particular segment or sequence of nucleotides alonga molecule of DNA (or RNA, in the case of RNA viruses) involved inproducing a polypeptide chain. The latter may be subjected to subsequentprocessing such as chemical modification, splicing and folding to obtaina functional protein or polypeptide. A gene may be isolated, partiallyisolated, or be found with an organism's genome. By way of example, atranscription factor gene encodes a transcription factor polypeptide,which may be functional or require processing to function as aninitiator of transcription.

Operationally, genes may be defined by the cis-trans test, a genetictest that determines whether two mutations occur in the same gene andthat may be used to determine the limits of the genetically active unit(Rieger et al. (1976) Glossary of Genetics and Cytogenetics: Classicaland Molecular, 4th ed., Springer Verlag. Berlin). A gene generallyincludes regions preceding (“leaders”; upstream) and following(“trailers”; downstream) the coding region. A gene may also includeintervening, non-coding sequences, referred to as “introns”, locatedbetween individual coding segments, referred to as “exons”. Most geneshave an associated promoter region, a regulatory sequence 5′ of thetranscription initiation codon (there are some genes that do not have anidentifiable promoter). The function of a gene may also be regulated byenhancers, operators, and other regulatory elements.

A “recombinant polynucleotide” is a polynucleotide that is not in itsnative state, for example, the polynucleotide comprises a nucleotidesequence not found in nature, or the polynucleotide is in a contextother than that in which it is naturally found, for example, separatedfrom nucleotide sequences with which it typically is in proximity innature, or adjacent (or contiguous with) nucleotide sequences with whichit typically is not in proximity. For example, the sequence at issue canbe cloned into a vector, or otherwise recombined with one or moreadditional nucleic acid.

An “isolated polynucleotide” is a polynucleotide, whether naturallyoccurring or recombinant, that is present outside the cell in which itis typically found in nature, whether purified or not. Optionally, anisolated polynucleotide is subject to one or more enrichment orpurification procedures, for example, cell lysis, extraction,centrifugation, precipitation, or the like.

A “polypeptide” is an amino acid sequence comprising a plurality ofconsecutive polymerized amino acid residues for example, at least about15 consecutive polymerized amino acid residues. In many instances, apolypeptide comprises a polymerized amino acid residue sequence that isa transcription factor or a domain or portion or fragment thereof.Additionally, the polypeptide may comprise: (i) a localization domain;(ii) an activation domain; (iii) a repression domain; (iv) anoligomerization domain; or (v) a DNA-binding domain, or the like. Thepolypeptide optionally comprises modified amino acid residues, naturallyoccurring amino acid residues not encoded by a codon, or non-naturallyoccurring amino acid residues.

“Protein” refers to an amino acid sequence, oligopeptide, peptide,polypeptide or portions thereof whether naturally occurring orsynthetic.

“Portion”, as used herein, refers to any part of a protein used for anypurpose, but especially for the screening of a library of molecules thatspecifically bind to that portion or for the production of antibodies.

A “recombinant polypeptide” is a polypeptide produced by translation ofa recombinant polynucleotide. A “synthetic polypeptide” is a polypeptidecreated by consecutive polymerization of isolated amino acid residuesusing methods well known in the art. An “isolated polypeptide,” whethera naturally occurring or a recombinant polypeptide, is more enriched in(or out of) a cell than the polypeptide in its natural state in awild-type cell, for example, more than about 5% enriched, or at least105% relative to wild type standardized at 100%. Such an enrichment isnot the result of a natural response of a wild-type plant.Alternatively, or additionally, the isolated polypeptide is separatedfrom other cellular components with which it is typically associated,for example, by any of the various protein purification methods herein.

“Homology” refers to sequence similarity between a reference sequenceand at least a fragment of a newly sequenced clone insert or its encodedamino acid sequence. Additionally, the terms “homology” and “homologoussequence(s)” may refer to one or more polypeptide sequences that aremodified by chemical or enzymatic means. The homologous sequence may bea sequence modified by lipids, sugars, peptides, organic or inorganiccompounds, by the use of modified amino acids or the like. Proteinmodification techniques are illustrated in Ausubel et al. (eds) CurrentProtocols in Molecular Biology, John Wiley & Sons (1998).

“Identity” or “similarity” refers to sequence similarity between twopolynucleotide sequences or between two polypeptide sequences, withidentity being a more strict comparison. The phrases “percent identity”and “% identity” refer to the percentage of sequence similarity found ina comparison of two or more polynucleotide sequences or two or morepolypeptide sequences. “Sequence similarity” refers to the percentsimilarity in base pair sequence (as determined by any suitable method)between two or more polynucleotide sequences. Two or more sequences canbe anywhere from 0-100% similar, or any integer value therebetween.Identity or similarity can be determined by comparing a position in eachsequence that may be aligned for purposes of comparison. When a positionin the compared sequence is occupied by the same nucleotide base oramino acid, then the molecules are identical at that position. A degreeof similarity or identity between polynucleotide sequences is a functionof the number of identical, matching of corresponding nucleotides atpositions shared by the polynucleotide sequences. A degree of identityof polypeptide sequences is a function of the number of identical aminoacids at corresponding positions shared by the polypeptide sequences. Adegree of homology or similarity of polypeptide sequences is a functionof the number of amino acids at corresponding positions shared by thepolypeptide sequences.

With regard to polypeptides, the terms “substantial identity” or“substantially identical” may refer to sequences of sufficientsimilarity and structure to the transcription factors in the SequenceListing to produce similar function when expressed or overexpressed in aplant; in the present invention, this function is altered C/N sensing orincreased tolerance to drought or shade. Sequences that are at leastabout 50% identical, and preferably at least 82% identical, to theinstant polypeptide sequences are considered to have “substantialidentity” with the latter. Sequences having lesser degrees of identitybut comparable biological activity are considered to be equivalents. Thestructure required to maintain proper functionality is related to thetertiary structure of the polypeptide. There are discreet domains andmotifs within a transcription factor that must be present within thepolypeptide to confer function and specificity. These specificstructures are required so that interactive sequences will be properlyoriented to retain the desired activity. “Substantial identity” may thusalso be used with regard to subsequences, for example, motifs, that areof sufficient structure and similarity, being at least about 50%identical, and preferably at least 82% identical, to similar motifs inother related sequences so that each confers or is required for alteredC/N sensing or increased tolerance to drought or shade.

The term “amino acid consensus motif” refers to the portion orsubsequence of a polypeptide sequence that is substantially conservedamong the polypeptide transcription factors listed in the SequenceListing.

“Alignment” refers to a number of nucleotide or amino acid residuesequences aligned by lengthwise comparison so that components in common(i.e., nucleotide bases or amino acid residues) may be visually andreadily identified. The fraction or percentage of components in commonis related to the homology or identity between the sequences. Alignmentssuch as those found the Figures may be used to identify conserveddomains and relatedness within these domains. An alignment may suitablybe determined by means of computer programs known in the art, such asMacVector (1999) (Accelrys, Inc., San Diego, Calif.).

A “conserved domain” or “conserved region” as used herein refers to aregion in heterologous polynucleotide or polypeptide sequences wherethere is a relatively high degree of sequence identity between thedistinct sequences. AP2 domains are examples of conserved domains.

With respect to polynucleotides encoding presently disclosedtranscription factors, a conserved domain is preferably at least 10 basepairs (bp) in length.

A “conserved domain”, with respect to presently disclosed polypeptidesrefers to a domain within a transcription factor family that exhibits ahigher degree of sequence homology, such as at least 70% sequencesimilarity, including conservative substitutions, and more preferably atleast 79% sequence identity, and even more preferably at least 81%, orat least about 86%, or at least about 87%, or at least about 89%, or atleast about 91%, or at least about 95%, or at least about 98% amino acidresidue sequence identity to the conserved domain. Sequences are alsoencompassed by the invention that possess or encode conserved domainsthat recognizable fall within a given clade of transcription factorpolypeptides and that have comparable biological activity to thesequences of this invention. A fragment or domain can be referred to asoutside a conserved domain, outside a consensus sequence, or outside aconsensus DNA-binding site that is known to exist or that exists for aparticular transcription factor class, family, or sub-family. In thiscase, the fragment or domain will not include the exact amino acids of aconsensus sequence or consensus DNA-binding site of a transcriptionfactor class, family or sub-family, or the exact amino acids of aparticular transcription factor consensus sequence or consensusDNA-binding site. Furthermore, a particular fragment, region, or domainof a polypeptide, or a polynucleotide encoding a polypeptide, can be“outside a conserved domain” if all the amino acids of the fragment,region, or domain fall outside of a defined conserved domain(s) for apolypeptide or protein. Sequences having lesser degrees of identity butcomparable biological activity are considered to be equivalents.

As one of ordinary skill in the art recognizes, conserved domains may beidentified as regions or domains of identity to a specific consensussequence (for example, Riechmann et al. (2000) supra). Thus, by usingalignment methods well known in the art, the conserved domains of theAP2 plant transcription factors may be determined.

The conserved domains for a number of the sequences that confer droughttolerance and altered C/N sensing are found in Tables 1 and 3,respectively. A comparison of the regions of the polypeptides in Table 1or 3 allows one of skill in the art to identify conserved domains forany of the polypeptides listed or referred to in this disclosure.

“Complementary” refers to the natural hydrogen bonding by base pairingbetween purines and pyrimidines. For example, the sequence A-C-G-T(5′->3′) forms hydrogen bonds with its complements A-C-G-T (5′->3′) orA-C-G-U (5′->3′). Two single-stranded molecules may be consideredpartially complementary, if only some of the nucleotides bond, or“completely complementary” if all of the nucleotides bond. The degree ofcomplementarity between nucleic acid strands affects the efficiency andstrength of hybridization and amplification reactions. “Fullycomplementary” refers to the case where bonding occurs between everybase pair and its complement in a pair of sequences, and the twosequences have the same number of nucleotides.

The terms “highly stringent” or “highly stringent condition” refer toconditions that permit hybridization of DNA strands whose sequences arehighly complementary, wherein these same conditions excludehybridization of significantly mismatched DNAs. Polynucleotide sequencescapable of hybridizing under stringent conditions with thepolynucleotides of the present invention may be, for example, variantsof the disclosed polynucleotide sequences, including allelic or splicevariants, or sequences that encode orthologs or paralogs of presentlydisclosed polypeptides. Nucleic acid hybridization methods are disclosedin detail by Kashima et al. (1985) Nature 313:402-404, Sambrook et al.(1989) Molecular Cloning: A Laboratory Manual, 2nd Ed., Cold SpringHarbor Laboratory, Cold Spring Harbor, N.Y. (“Sambrook”), and by Hamesand Higgins, “Nucleic Acid Hybridisation: A Practical Approach”, IRLPress, Washington, D.C. (1985), which references are incorporated hereinby reference.

In general, stringency is determined by the temperature, ionic strength,and concentration of denaturing agents (for example, formamide) used ina hybridization and washing procedure (for a more detailed descriptionof establishing and determining stringency, see below). The degree towhich two nucleic acids hybridize under various conditions of stringencyis correlated with the extent of their similarity. Thus, similar nucleicacid sequences from a variety of sources, such as within a plant'sgenome (as in the case of paralogs) or from another plant (as in thecase of orthologs) that may perform similar functions can be isolated onthe basis of their ability to hybridize with known transcription factorsequences. Numerous variations are possible in the conditions and meansby which nucleic acid hybridization can be performed to isolatetranscription factor sequences having similarity to transcription factorsequences known in the art and are not limited to those explicitlydisclosed herein. Such an approach may be used to isolate polynucleotidesequences having various degrees of similarity with disclosedtranscription factor sequences, such as, for example, transcriptionfactors having 60% identity, or more preferably greater than about 70%identity, most preferably 72% or greater identity with disclosedtranscription factors.

Regarding the terms “paralog” and “ortholog”, homologous polynucleotidesequences and homologous polypeptide sequences may be paralogs ororthologs of the claimed polynucleotide or polypeptide sequence.Orthologs and paralogs are evolutionarily-related genes that havesimilar sequence and similar functions. Orthologs are structurallyrelated genes in different species that are derived by a speciationevent. Paralogs are structurally related genes within a single speciesthat are derived by a duplication event. Sequences that are sufficientlysimilar to one another will be appreciated by those of skill in the artand may be based upon percentage identity of the complete sequences,percentage identity of a conserved domain or sequence within thecomplete sequence, percentage similarity to the complete sequence,percentage similarity to a conserved domain or sequence within thecomplete sequence, and/or an arrangement of contiguous nucleotides orpeptides particular to a conserved domain or complete sequence.Sequences that are sufficiently similar to one another will also bind ina similar manner to the same DNA binding sites of transcriptionalregulatory elements using methods well known to those of skill in theart.

The term “equivalog” describes members of a set of homologous proteinsthat are conserved with respect to function since their last commonancestor. Related proteins are grouped into equivalog families, andotherwise into protein families with other hierarchically definedhomology types. This definition is provided at the Institute for GenomicResearch (TIGR) world wide web (www) website, “tigr.org” under theheading “Terms associated with TIGRFAMs”.

The term “variant”, as used herein, may refer to polynucleotides orpolypeptides that differ from the presently disclosed polynucleotides orpolypeptides, respectively, in sequence from each other, and as setforth below.

With regard to polynucleotide variants, differences between presentlydisclosed polynucleotides and polynucleotide variants are limited sothat the nucleotide sequences of the former and the latter are closelysimilar overall and, in many regions, identical. Due to the degeneracyof the genetic code, differences between the former and latternucleotide sequences may be silent (i.e., the amino acids encoded by thepolynucleotide are the same, and the variant polynucleotide sequenceencodes the same amino acid sequence as the presently disclosedpolynucleotide. Variant nucleotide sequences may encode different aminoacid sequences, in which case such nucleotide differences will result inamino acid substitutions, additions, deletions, insertions, truncationsor fusions with respect to the similar disclosed polynucleotidesequences. These variations may result in polynucleotide variantsencoding polypeptides that share at least one functional characteristic.The degeneracy of the genetic code also dictates that many differentvariant polynucleotides can encode identical and/or substantiallysimilar polypeptides in addition to those sequences illustrated in theSequence Listing.

Presently disclosed polypeptide sequences and similar polypeptidevariants may differ in amino acid sequence by one or more substitutions,additions, deletions, fusions and truncations, which may be present inany combination. These differences may produce silent changes and resultin a functionally equivalent transcription factor. Thus, it will bereadily appreciated by those of skill in the art, that any of a varietyof polynucleotide sequences is capable of encoding the transcriptionfactors and transcription factor homolog polypeptides of the invention.A polypeptide sequence variant may have “conservative” changes, whereina substituted amino acid has similar structural or chemical properties.Deliberate amino acid substitutions may thus be made on the basis ofsimilarity in polarity, charge, solubility, hydrophobicity,hydrophilicity, and/or the amphipathic nature of the residues, as longas a substantial amount of the functional or biological activity of thetranscription factor is retained. For example, negatively charged aminoacids may include aspartic acid and glutamic acid, positively chargedamino acids may include lysine and arginine, and amino acids withuncharged polar head groups having similar hydrophilicity values mayinclude leucine, isoleucine, and valine; glycine and alanine; asparagineand glutamine; serine and threonine; and phenylalanine and tyrosine (formore detail on conservative substitutions, see Table 6). More rarely, avariant may have “non-conservative” changes, for example, replacement ofa glycine with a tryptophan. Similar minor variations may also includeamino acid deletions or insertions, or both. Related polypeptides maycomprise, for example, additions and/or deletions of one or moreN-linked or O-linked glycosylation sites, or an addition and/or adeletion of one or more cysteine residues. Guidance in determining whichand how many amino acid residues may be substituted, inserted or deletedwithout abolishing functional or biological activity may be found usingcomputer programs well known in the art, for example, DNASTAR software(U.S. Pat. No. 5,840,544).

Also within the scope of the invention is a variant of a transcriptionfactor nucleic acid listed in the Sequence Listing, that is, one havinga sequence that differs from the one of the polynucleotide sequences inthe Sequence Listing, or a complementary sequence, that encodes afunctionally equivalent polypeptide (i.e., a polypeptide having somedegree of equivalent or similar biological activity) but differs insequence from the sequence in the Sequence Listing, due to degeneracy inthe genetic code. Included within this definition are polymorphisms thatmay or may not be readily detectable using a particular oligonucleotideprobe of the polynucleotide encoding polypeptide, and improper orunexpected hybridization to allelic variants, with a locus other thanthe normal chromosomal locus for the polynucleotide sequence encodingpolypeptide.

“Allelic variant” or “polynucleotide allelic variant” refers to any oftwo or more alternative forms of a gene occupying the same chromosomallocus. Allelic variation arises naturally through mutation, and mayresult in phenotypic polymorphism within populations. Gene mutations maybe “silent” or may encode polypeptides having altered amino acidsequence. “Allelic variant” and “polypeptide allelic variant” may alsobe used with respect to polypeptides, and in this case the term refer toa polypeptide encoded by an allelic variant of a gene.

“Splice variant” or “polynucleotide splice variant” as used hereinrefers to alternative forms of RNA transcribed from a gene. Splicevariation naturally occurs as a result of alternative sites beingspliced within a single transcribed RNA molecule or between separatelytranscribed RNA molecules, and may result in several different forms ofmRNA transcribed from the same gene. Thus, splice variants may encodepolypeptides having different amino acid sequences, which may or may nothave similar functions in the organism. “Splice variant” or “polypeptidesplice variant” may also refer to a polypeptide encoded by a splicevariant of a transcribed mRNA.

As used herein, “polynucleotide variants” may also refer topolynucleotide sequences that encode paralogs and orthologs of thepresently disclosed polypeptide sequences. “Polypeptide variants” mayrefer to polypeptide sequences that are paralogs and orthologs of thepresently disclosed polypeptide sequences.

“Ligand” refers to any molecule, agent, or compound that will bindspecifically to a complementary site on a nucleic acid molecule orprotein. Such ligands stabilize or modulate the activity of nucleic acidmolecules or proteins of the invention and may be composed of at leastone of the following: inorganic and organic substances including nucleicacids, proteins, carbohydrates, fats, and lipids.

“Modulates” refers to a change in activity (biological, chemical, orimmunological) or lifespan resulting from specific binding between amolecule and either a nucleic acid molecule or a protein.

The term “plant” includes whole plants, shoot vegetativeorgans/structures (for example, leaves, stems and tubers), roots,flowers and floral organs/structures (for example, bracts, sepals,petals, stamens, carpels, anthers and ovules), seed (including embryo,endosperm, and seed coat) and fruit (the mature ovary), plant tissue(for example, vascular tissue, ground tissue, and the like) and cells(for example, guard cells, egg cells, and the like), and progeny ofsame. The class of plants that can be used in the method of theinvention is generally as broad as the class of higher and lower plantsamenable to transformation techniques, including angiosperms(monocotyledonous and dicotyledonous plants), gymnosperms, ferns,horsetails, psilophytes, lycophytes, bryophytes, and multicellular algae(as shown, for example, in FIG. 1, adapted from Daly et al. (2001) PlantPhysiol. 127: 1328-1333, and in FIG. 2, adapted from Ku et al. (2000)Proc. Natl. Acad. Sci. 97: 9121-9126; and in Tudge (2000) in The Varietyof Life, Oxford University Press, New York, N.Y., pp. 547-606).

A “transgenic plant” refers to a plant that contains genetic materialnot found in a wild-type plant of the same species, variety or cultivar.The genetic material may include a transgene, an insertional mutagenesisevent (such as by transposon or T-DNA insertional mutagenesis), anactivation tagging sequence, a mutated sequence, a homologousrecombination event or a sequence modified by chimeraplasty. Typically,the foreign genetic material has been introduced into the plant by humanmanipulation, but any method can be used as one of skill in the artrecognizes.

A transgenic plant may contain an expression vector or cassette. Theexpression cassette typically comprises a polypeptide-encoding sequenceoperably linked (i.e., under regulatory control of) to appropriateinducible or constitutive regulatory sequences that allow for theexpression of polypeptide. The expression cassette can be introducedinto a plant by transformation or by breeding after transformation of aparent plant. A plant refers to a whole plant as well as to a plantpart, such as seed, fruit, leaf, or root, plant tissue, plant cells orany other plant material, for example, a plant explant, as well as toprogeny thereof, and to in vitro systems that mimic biochemical orcellular components or processes in a cell.

“Wild type” or “wild-type”, as used herein, refers to a plant cell,seed, plant component, plant tissue, plant organ or whole plant that hasnot been genetically modified or treated in an experimental sense.Wild-type cells, seed, components, tissue, organs or whole plants may beused as controls to compare levels of expression and the extent andnature of trait modification with cells, tissue or plants of the samespecies in which a transcription factor expression is altered, forexample, in that it has been knocked out, overexpressed, or ectopicallyexpressed.

A “control plant” as used in the present invention refers to a plantcell, seed, plant component, plant tissue, plant organ or whole plantused to compare against transgenic or genetically modified plant for thepurpose of identifying an enhanced phenotype in the transgenic orgenetically modified plant. A control plant may in some cases be atransgenic plant line that comprises an empty vector or marker gene, butdoes not contain the recombinant polynucleotide of the present inventionthat is expressed in the transgenic or genetically modified plant beingevaluated. In general, a control plant is a plant of the same line orvariety as the transgenic or genetically modified plant being tested. Asuitable control plant would include a genetically unaltered ornon-transgenic plant of the parental line used to generate a transgenicplant herein.

“Fragment”, with respect to a polynucleotide, refers to a clone or anypart of a polynucleotide molecule that retains a usable, functionalcharacteristic. Useful fragments include oligonucleotides andpolynucleotides that may be used in hybridization or amplificationtechnologies or in the regulation of replication, transcription ortranslation. A “polynucleotide fragment” refers to any subsequence of apolynucleotide, typically, of at least about nine consecutivenucleotides, preferably at least about 30 nucleotides, more preferablyat least about 50 nucleotides, of any of the sequences provided herein.Exemplary polynucleotide fragments are the first sixty consecutivenucleotides of the transcription factor polynucleotides listed in theSequence Listing. Exemplary fragments include fragments comprising aregion that encodes a conserved domain (for example, an AP2 domain) of atranscription factor.

Fragments may also include subsequences of polypeptides and proteinmolecules, or a subsequence of the polypeptide. Fragments may have usesin that they may have antigenic potential. In some cases, the fragmentor domain is a subsequence of the polypeptide which performs at leastone biological function of the intact polypeptide in substantially thesame manner, or to a similar extent, as does the intact polypeptide. Forexample, a polypeptide fragment can comprise a recognizable structuralmotif or functional domain such as a DNA-binding site or domain thatbinds to a DNA promoter region, an activation domain, or a domain forprotein-protein interactions, and may initiate transcription. Fragmentscan vary in size from as few as 3 amino acid residues to the full lengthof the intact polypeptide, but are preferably at least about 30 aminoacid residues in length and more preferably at least about 60 amino acidresidues in length. Exemplary polypeptide fragments are the first twentyconsecutive amino acids of the transcription factor polypeptides listedin the Sequence Listing. Exemplary fragments also include fragments thatcomprise an AP2 domain of a transcription factor, for example, aminoacid residues 10-77 of G2133 (SEQ ID NO: 12), as noted in Table 1.

The invention also encompasses production of DNA sequences that encodetranscription factors and transcription factor derivatives, or fragmentsthereof, entirely by synthetic chemistry. After production, thesynthetic sequence may be inserted into any of the many availableexpression vectors and cell systems using reagents well known in theart. Moreover, synthetic chemistry may be used to introduce mutationsinto a sequence encoding transcription factors or any fragment thereof.

“Derivative” refers to the chemical modification of a nucleic acidmolecule or amino acid sequence. Chemical modifications can includereplacement of hydrogen by an alkyl, acyl, or amino group orglycosylation, pegylation, or any similar process that retains orenhances biological activity or lifespan of the molecule or sequence.

A “trait” refers to a physiological, morphological, biochemical, orphysical characteristic of a plant or particular plant material or cell.In some instances, this characteristic is visible to the human eye, suchas seed or plant size, or can be measured by biochemical techniques,such as detecting the protein, starch, or oil content of seed or leaves,or by observation of a metabolic or physiological process, for example,by measuring tolerance to water deprivation or particular salt or sugarconcentrations, or by the observation of the expression level of a geneor genes, for example, by employing Northern analysis, RT-PCR,microarray gene expression assays, or reporter gene expression systems,or by agricultural observations such as drought stress tolerance oryield. Any technique can be used to measure the amount of, comparativelevel of, or difference in any selected chemical compound ormacromolecule in the transgenic plants, however.

“Trait modification” refers to a detectable difference in acharacteristic in a plant ectopically expressing a polynucleotide orpolypeptide of the present invention relative to a plant not doing so,such as a wild-type plant. In some cases, the trait modification can beevaluated quantitatively. For example, the trait modification can entailat least about a 2% increase or decrease in an observed trait, or aneven greater difference, as compared with a wild-type or control plant.It is known that there can be a natural variation in the modified trait.Therefore, the trait modification observed entails a change of thenormal distribution and magnitude of the trait in the plants comparedwith the distribution and magnitude observed in wild-type plants.

The term “transcript profile” refers to the expression levels of a setof genes in a cell in a particular state, particularly by comparisonwith the expression levels of that same set of genes in a cell of thesame type in a reference state. For example, the transcript profile of aparticular transcription factor in a suspension cell is the expressionlevels of a set of genes in a cell repressing or overexpressing thattranscription factor compared with the expression levels of that sameset of genes in a suspension cell that has normal levels of thattranscription factor. The transcript profile can be presented as a listof those genes whose expression level is significantly different betweenthe two treatments, and the difference ratios. Differences andsimilarities between expression levels may also be evaluated andcalculated using statistical and clustering methods.

“Ectopic expression or altered expression” in reference to apolynucleotide indicates that the pattern of expression in, for example,a transgenic plant or plant tissue, is different from the expressionpattern in a wild-type plant or a reference plant of the same species.The pattern of expression may also be compared with a referenceexpression pattern in a wild-type plant of the same species. Forexample, the polynucleotide or polypeptide is expressed in a cell ortissue type other than a cell or tissue type in which the sequence isexpressed in the wild-type plant, or by expression at a time other thanat the time the sequence is expressed in the wild-type plant, or by aresponse to different inducible agents, such as hormones orenvironmental signals, or at different expression levels (either higheror lower) compared with those found in a wild-type plant. The term alsorefers to altered expression patterns that are produced by lowering thelevels of expression to below the detection level or completelyabolishing expression. The resulting expression pattern can be transientor stable, constitutive or inducible. In reference to a polypeptide, theterm “ectopic expression or altered expression” further may relate toaltered activity levels resulting from the interactions of thepolypeptides with exogenous or endogenous modulators or frominteractions with factors or as a result of the chemical modification ofthe polypeptides.

The term “overexpression” as used herein refers to a greater expressionlevel of a gene in a plant, plant cell or plant tissue, compared toexpression in a wild-type plant, cell or tissue, at any developmental ortemporal stage for the gene. Overexpression can occur when, for example,the genes encoding one or more transcription factors are under thecontrol of a strong promoter described herein (for example, thecauliflower mosaic virus 35S transcription initiation region), oroverexpression can be induced when an appropriate environmental signalis present. Overexpression may occur throughout a plant or in specifictissues of the plant, depending on the promoter used, as describedbelow.

Overexpression may take place in plant cells normally lacking expressionof polypeptides functionally equivalent or identical to the presenttranscription factors. Overexpression may also occur in plant cellswhere endogenous expression of the present transcription factors orfunctionally equivalent molecules normally occurs, but such normalexpression is at a lower level. Overexpression thus results in a greaterthan normal production, or “overproduction” of the transcription factorin the plant, cell or tissue.

The term “transcription regulating region” refers to a DNA regulatorysequence that regulates expression of one or more genes in a plant whena transcription factor having one or more specific binding domains bindsto the DNA regulatory sequence. Transcription factors of the presentinvention may possess, for example, an AP2 domain, in which case the AP2domain of the transcription factor binds to a transcription regulatingregion, such as AtERF1, which binds to the motif AGCCGCC (the “GCC box”)that are present in promoters of genes such as PDF1.2. The transcriptionfactors of the invention also comprise an amino acid subsequence thatforms a transcription activation domain that regulates expression of oneor more abiotic stress tolerance genes in a plant when the transcriptionfactor binds to the regulating region.

A “sample” with respect to a material containing nucleic acid moleculesmay comprise a bodily fluid; an extract from a cell, chromosome,organelle, or membrane isolated from a cell; genomic DNA, RNA, or cDNAin solution or bound to a substrate; a cell; a tissue; a tissue print; aforensic sample; and the like. In this context “substrate” refers to anyrigid or semi-rigid support to which nucleic acid molecules or proteinsare bound and includes membranes, filters, chips, slides, wafers,fibers, magnetic or nonmagnetic beads, gels, capillaries or othertubing, plates, polymers, and microparticles with a variety of surfaceforms including wells, trenches, pins, channels and pores. A substratemay also refer to a reactant in a chemical or biological reaction, or asubstance acted upon (for example, by an enzyme).

Transcription Factors Modify Expression of Endogenous Genes

A transcription factor may include, but is not limited to, anypolypeptide that can activate or repress transcription of a single geneor a number of genes. As one of ordinary skill in the art recognizes,transcription factors can be identified by the presence of a region ordomain of structural similarity or identity to a specific consensussequence or the presence of a specific consensus DNA-binding site orDNA-binding site motif (for example, in Riechmann et al. (2000) Science290: 2105-2110).

Generally, the transcription factors encoded by the present sequencesare involved in cell differentiation and proliferation and theregulation of growth. Accordingly, one skilled in the art wouldrecognize that by expressing the present sequences in a plant, one maychange the expression of autologous genes or induce the expression ofintroduced genes. By affecting the expression of similar autologoussequences in a plant that have the biological activity of the presentsequences, or by introducing the present sequences into a plant, one mayalter a plant's phenotype to one with improved traits related to droughtstress, shade tolerance or C/N sensing. The sequences of the inventionmay also be used to transform a plant and introduce desirable traits notfound in the wild-type cultivar or strain. Plants may then be selectedfor those that produce the most desirable degree of over- orunder-expression of target genes of interest and coincident traitimprovement.

The sequences of the present invention may be from any species,particularly plant species, in a naturally-occurring form or from anysource whether natural, synthetic, semi-synthetic or recombinant. Thesequences of the invention may also include fragments of the presentamino acid sequences. Where “amino acid sequence” is recited to refer toan amino acid sequence of a naturally occurring protein molecule, “aminoacid sequence” and like terms are not meant to limit the amino acidsequence to the complete native amino acid sequence associated with therecited protein molecule.

In addition to methods for modifying a plant phenotype by employing oneor more polynucleotides and polypeptides of the invention describedherein, the polynucleotides and polypeptides of the invention have avariety of additional uses. These uses include their use in therecombinant production (i.e., expression) of proteins; as regulators ofplant gene expression, as diagnostic probes for the presence ofcomplementary or partially complementary nucleic acids (including fordetection of natural coding nucleic acids); as substrates for furtherreactions, for example, mutation reactions, PCR reactions, or the like;as substrates for cloning for example, including digestion or ligationreactions; and for identifying exogenous or endogenous modulators of thetranscription factors. In many instances, a polynucleotide comprises anucleotide sequence encoding a polypeptide (or protein) or a domain orfragment thereof. Additionally, the polynucleotide may comprise apromoter, an intron, an enhancer region, a polyadenylation site, atranslation initiation site, 5′ or 3′ untranslated regions, a reportergene, a selectable marker, or the like. The polynucleotide can besingle-stranded or double-stranded DNA or RNA. The polynucleotideoptionally comprises modified bases or a modified backbone. Thepolynucleotide can be, for example, genomic DNA or RNA, a transcript(such as an mRNA), a cDNA, a PCR product, a cloned DNA, a synthetic DNAor RNA, or the like. The polynucleotide can comprise a sequence ineither sense or antisense orientations.

Expression of genes that encode transcription factors that modifyexpression of endogenous genes, polynucleotides, and proteins are wellknown in the art. In addition, transgenic plants comprising isolatedpolynucleotides encoding transcription factors may also modifyexpression of endogenous genes, polynucleotides, and proteins. Examplesinclude Peng et al. (1997) Genes Development 11: 3194-3205, and Peng etal. (1999) Nature, 400: 256-261). In addition, many others havedemonstrated that an Arabidopsis transcription factor expressed in anexogenous plant species elicits the same or very similar phenotypicresponse (for example, in Fu et al. (2001) Plant Cell 13: 1791-1802;Nandi et al. (2000) Curr. Biol. 10: 215-218; Coupland (1995) Nature 377:482-483; and Weigel and Nilsson (1995) Nature 377: 482-500).

In another example, Mandel et al. (1992) Cell 71-133-143, and Suzuki etal. (2001) Plant J. 28: 409-418 teach that a transcription factorexpressed in another plant species elicits the same or very similarphenotypic response of the endogenous sequence, as often predicted inearlier studies of Arabidopsis transcription factors in Arabidopsis(Mandel et al. (1992) supra; and Suzuki et al. (2001) supra). Otherexamples include Müller et al. (2001) Plant J. 28: 169-179; Kim et al.(2001) Plant J. 25: 247-259; Kyozuka and Shimamoto (2002) Plant CellPhysiol. 43: 130-135; Boss and Thomas (2002) Nature, 416: 847-850; He etal. (2000) Transgenic Res. 9: 223-227; and Robson et al. (2001) Plant J.28: 619-631.

In yet another example, Gilmour et al. (1998) Plant J. 16: 433-442,teach an Arabidopsis AP2 transcription factor, CBF1, which, whenoverexpressed in transgenic plants, increases plant freezing tolerance.Jaglo et al. (2001) Plant Physiol. 127: 910-917, further identifiedsequences in Brassica napus which encode CBF-like genes and thattranscripts for these genes accumulated rapidly in response to lowtemperature. Transcripts encoding CBF-like proteins were also found toaccumulate rapidly in response to low temperature in wheat, as well asin tomato. An alignment of the CBF proteins from Arabidopsis, B. napus,wheat, rye, and tomato revealed the presence of conserved consecutiveamino acid residues, PKK/RPAGRxKFxETRHP (SEQ ID NO: 1260) and DSAWR (SEQID NO: 1261), that bracket the AP2/EREBP DNA binding domains of theproteins and distinguish them from other members of the AP2/EREBPprotein family (Jaglo et al. (2001) supra).

Transcription factors mediate cellular responses and control traitsthrough altered expression of genes containing cis-acting nucleotidesequences that are targets of the introduced transcription factor. It iswell appreciated in the art that the effect of a transcription factor oncellular responses or a cellular trait is determined by the particulargenes whose expression is either directly or indirectly (for example, bya cascade of transcription factor binding events and transcriptionalchanges) altered by transcription factor binding. In a global analysisof transcription comparing a standard condition with one in which atranscription factor is overexpressed, the resulting transcript profileassociated with transcription factor overexpression is related to thetrait or cellular process controlled by that transcription factor. Forexample, the PAP2 gene (and other genes in the MYB family) have beenshown to control anthocyanin biosynthesis through regulation of theexpression of genes known to be involved in the anthocyanin biosyntheticpathway (Bruce et al. (2000) Plant Cell, 12: 65-79; Borevitz et al.(2000) Plant Cell 12: 2383-93). Further, global transcript profiles havebeen used successfully as diagnostic tools for specific cellular states(for example, cancerous vs. non-cancerous; Bhattacharjee et al. (2001)Proc Natl. Acad. Sci., USA, 98: 13790-13795; Xu et al. (2001) Proc.Natl. Acad. Sci., USA, 98: 15089-15094). Consequently, it is evident toone skilled in the art that similarity of transcript profile uponoverexpression of different transcription factors would indicatesimilarity of transcription factor function.

Polypeptides and Polynucleotides of the Invention

The present invention provides, among other things, transcriptionfactors (TFs), and transcription factor homolog polypeptides, andisolated or recombinant polynucleotides encoding the polypeptides, ornovel sequence variant polypeptides or polynucleotides encoding novelvariants of transcription factors derived from the specific sequencesprovided here.

The polynucleotides of the invention can be or were ectopicallyexpressed in overexpressor plant cells and the changes in the expressionlevels of a number of genes, polynucleotides, and/or proteins of theplant cells observed. Therefore, the polynucleotides and polypeptidescan be employed to change expression levels of a genes, polynucleotides,and/or proteins of plants or plant cells. These polypeptides andpolynucleotides may be employed to modify a plant's characteristics,particularly drought tolerance, shade tolerance, and/or C/N sensing. Thepolynucleotides of the invention can be or were ectopically expressed inoverexpressor or knockout plants and the changes in thecharacteristic(s) or trait(s) of the plants observed. Therefore, thepolynucleotides and polypeptides can be employed to improve thecharacteristics of plants. The polypeptide sequences of the sequencelisting have been shown to confer increased drought or shade toleranceor altered C/N sensing when these polypeptides are overexpressed inArabidopsis plants. These polynucleotides have been shown to have astrong association with these traits, in that plants that overexpressthese sequences are more tolerant to drought, shade, or have altered C/Nsensing, respectively. The invention also encompasses a complement ofthe polynucleotides. The polynucleotides are also useful for screeninglibraries of molecules or compounds for specific binding and forcreating transgenic plants having improved traits. Altering theexpression levels of equivalogs of these sequences, including paralogsand orthologs in the Sequence Listing, and other orthologs that arestructurally and sequentially similar to the former orthologs, has beenshown and is expected to confer similar phenotypes, including alteredC/N sensing, drought and/or shade tolerance in plants.

In some cases, exemplary polynucleotides encoding the polypeptides ofthe invention were identified in the Arabidopsis thaliana GenBankdatabase using publicly available sequence analysis programs andparameters. Sequences initially identified were then furthercharacterized to identify sequences comprising specified sequencestrings corresponding to sequence motifs present in families of knowntranscription factors. In addition, further exemplary polynucleotidesencoding the polypeptides of the invention were identified in the plantGenBank database using publicly available sequence analysis programs andparameters. Sequences initially identified were then furthercharacterized to identify sequences comprising specified sequencestrings corresponding to sequence motifs present in families of knowntranscription factors. Polynucleotide sequences meeting such criteriawere confirmed as transcription factors.

Additional polynucleotides of the invention were identified by screeningArabidopsis thaliana and/or other plant cDNA libraries with probescorresponding to known transcription factors under low stringencyhybridization conditions. Additional sequences, including full lengthcoding sequences were subsequently recovered by the rapid amplificationof cDNA ends (RACE) procedure, using a commercially available kitaccording to the manufacturer's instructions. Where necessary, multiplerounds of RACE are performed to isolate 5′ and 3′ ends. The full-lengthcDNA was then recovered by a routine end-to-end polymerase chainreaction (PCR) using primers specific to the isolated 5′ and 3′ ends.Exemplary sequences are provided in the Sequence Listing.

The polynucleotides are particularly useful when they are hybridizablearray elements in a microarray. Such a microarray can be employed tomonitor the expression of genes that are differentially expressed inresponse to limited light, drought, other osmotic stresses, or lownitrogen availability. The microarray can be used in large scale geneticor gene expression analysis of a large number of polynucleotides; or inthe diagnosis of, for example, drought stress before phenotypic symptomsare evident. Furthermore, the microarray can be employed to investigatecellular responses, such as cell proliferation, transformation, and thelike.

When the polynucleotides of the invention may also be used ashybridizable array elements in a microarray, the array elements areorganized in an ordered fashion so that each element is present at aspecified location on the substrate. Because the array elements are atspecified locations on the substrate, the hybridization patterns andintensities (which together create a unique expression profile) can beinterpreted in terms of expression levels of particular genes and can becorrelated with a particular stress, pathology, or treatment.

The invention also entails an agronomic composition comprising apolynucleotide of the invention in conjunction with a suitable carrierand a method for altering a plant's trait using the composition.

Examples of specific polynucleotide and polypeptides of the invention,and equivalog sequences, along with descriptions of the gene familiesthat comprise these polynucleotides and polypeptides, are providedbelow.

Examples of specific polynucleotide and polypeptides of the invention,and equivalog sequences, are provided below.

Polypeptide sequences of the sequence listing, including, for example,Arabidopsis sequences G2133, G1274, G922, G2999, G3086, G354, G1792,G2053, G975, G1069, G916, G1820, G2701, G47, G2854, G2789, G634, G175,G2839, G1452, G3083, G489, G303, G2992, and G682 (SEQ ID NOs: 12, 6, 4,14, 16, 228, 8, 10, 238, 240, 236, 244, 246, 2, 252, 248, 232, 224, 250,242, 254, 230, 226, 50 and 234, respectively) have been shown to conferincreased drought tolerance when expression of these polypeptides isaltered in Arabidopsis plants. These polynucleotides have been shown tohave a strong association with drought stress tolerance, in that plantsthat overexpress these sequences are more tolerant to drought. Exemplarysequences of the invention include G2133, G47, and structurally andfunctionally-related sequences found in the G47 clade of transcriptionfactor polypeptides (examples of which may be found in FIGS. 3 and 4).

A number of the polypeptide sequences of the sequence listing,including, for example, G682, G226, G1816, G2718, G24, G154, G384, G486,G545, G760, G773, G937, G971, G988, G989, G1069, G1090, G1322, G1587,G1666, G1700, G1818, G1868, G1888, G2117, G2131, G2520, G2522, G2789,G8, G27, G156, G161, G168, G183, G189, G200, G234, G237, G275, G326,G347, G427, G505, G590, G602, G618, G635, G643, G653, G657, G837, G866,G872, G904, G912, G932, G958, G964, G975, G979, G1049, G1246, G1255,G1266, G1331, G1332, G1494, G1535, G1649, G1750, G1773, G1835, G1930,G2053, G2057, G2133, G2144, G2145, G2295, G2512, G2531, G2535, G2590,and G2719 (SEQ ID NOs: 234, 286, 312, 324, 420, 422, 424, 294, 426, 428,430, 432, 434, 436, 438, 240, 440, 442, 444, 446, 448, 450, 452, 454,456, 458, 460, 462, 248, 464, 466, 468, 470, 472, 474, 476, 478, 480,482, 484, 486, 488, 490, 492, 494, 496, 498, 500, 502, 504, 506, 508,510, 512, 514, 516, 518, 520, 522, 238, 524, 526, 528, 530, 532, 534,536, 538, 540, 542, 544, 546, 548, 550, 10, 552, 12, 554, 556, 558, 560,562, 564, 566, and 568, respectively) have been shown to confer alteredC/N sensing when expression of these polypeptides is altered inArabidopsis plants. A number of these polynucleotides have also beenshown to confer increased tolerance to low nutrient (e.g.,nitrogen-limited) environments and other abiotic stress tolerances suchas drought, heat, and cold. Exemplary sequences of the invention includeG682 and structurally and functionally-related sequences found in theG682 subclade (examples may be found in FIGS. 20A, 20B and 21).

A number of the polypeptide sequences of the sequence listing,including, for example, G634, G1048, G1100, G1412, G2505, G1796, G1995,G2467, G2550, G2640, G2686, and G2789 (SEQ ID NOs: 232, 808, 810, 658,818, 812, 814, 816, 820, 822, 824 and 248, respectively) have also beenshown to confer increased shade tolerance when expression of thesepolypeptides is altered in Arabidopsis plants. Equivalogs of thesesequences, including paralogs and orthologs in the Sequence Listing, andother orthologs that are structurally and sequentially similar to theformer orthologs, are expected to confer increased shade tolerance inplants when their expression is altered. Exemplary sequences of theinvention include G634 and structurally and functionally-relatedsequences found in the 6634 clade (examples of which may be found inTable 8).

The invention also encompasses the complements of these polynucleotides.The polynucleotides are also useful for screening libraries of moleculesor compounds for specific binding and for creating transgenic plantshaving altered C/N sensing or increased abiotic stress or shadetolerance. Equivalogs of these sequences, including paralogs andorthologs in the Sequence Listing, and other orthologs that arestructurally and sequentially similar to the former orthologs, areexpected to confer altered C/N sensing and/or abiotic stress tolerancein plants when their expression is altered.

The AP2 Family, Including the G47/G2133 and G1792 Clades.

AP2 (APETALA2) and EREBPs (Ethylene-Responsive Element Binding Proteins)are the prototypic members of a family of transcription factors uniqueto plants, whose distinguishing characteristic is that they contain theso-called AP2 DNA-binding domain (Riechmann and Meyerowitz (1998) Biol.Chem. 379: 633-646). The AP2 domain was first recognized as a repeatedmotif within the Arabidopsis thaliana AP2 protein (Jofuku et al. (1994)Plant Cell 6: 1211-1225). Shortly afterwards, four DNA-binding proteinsfrom tobacco were identified that interact with a sequence that isessential for the responsiveness of some promoters to the plant hormoneethylene, and were designated as ethylene-responsive element bindingproteins (EREBPs; Ohme-Takagi et al. (1995) Plant Cell 7: 173-182). TheDNA-binding domain of EREBP-2 was mapped to a region that was common toall four proteins (Ohme-Takagi et al (1995) supra), and that was foundto be closely related to the AP2 domain (Weigel (1995) Plant Cell 7:388-389) but that did not bear sequence similarity to previously knownDNA-binding motifs.

AP2/EREBP genes form a large family, with many members known in severalplant species (Okamuro et al. (1997) Proc. Natl. Acad. Sci. USA 94:7076-7081; Riechmann and Meyerowitz (1998) supra). The number ofAP2/EREBP genes in the Arabidopsis thaliana genome is approximately 145(Riechmann et al. (2000) Science 290: 2105-2110). The APETALA2 class ischaracterized by the presence of two AP2 DNA binding domains, andcontains 14 genes. The AP2/ERF is the largest subfamily, and includes125 genes which are involved in abiotic (DREB subgroup) and biotic (ERFsubgroup) stress responses and the RAV subgroup includes 6 genes whichall have a B3 DNA binding domain in addition to the AP2 DNA bindingdomain (Kagaya et al. (1999) Nucleic Acids Res. 27: 470-478).

Arabidopsis AP2 is involved in the specification of sepal and petalidentity through its activity as a homeotic gene that forms part of thecombinatorial genetic mechanism of floral organ identity determinationand it is also required for normal ovule and seed development (Bowman etal. (1991) Development 112: 1-20; Jofuku et al. (1994) supra).Arabidopsis ANT is required for ovule development and it also plays arole in floral organ growth (Elliott et al. (1996) Plant Cell 8:155-168; Klucher et al. (1996) Plant Cell 8: 137-153). Finally, maizeG115 regulates leaf epidermal cell identity (Moose et al. (1996) GenesDev. 10: 3018-3027).

The attack of a plant by a pathogen may induce defense responses thatlead to resistance to the invasion, and these responses are associatedwith transcriptional activation of defense-related genes, among themthose encoding pathogenesis-related (PR) proteins. The involvement ofEREBP-like genes in controlling the plant defense response is based onthe observation that many PR gene promoters contain a short cis-actingelement that mediates their responsiveness to ethylene (ethylene appearsto be one of several signal molecules controlling the activation ofdefense responses). Tobacco EREBP-1, -2, -3, and -4, and tomato Pti4,Pti5 and Pti6 proteins have been shown to recognize such cis-actingelements (Ohme-Takagi (1995) supra; Zhou et al. (1997) EMBO J. 16:3207-3218). In addition, Pti4, Pti5, and Pti6 proteins have been shownto directly interact with Pto, a protein kinase that confers resistanceagainst Pseudomonas syringae pv tomato (Zhou et al. (1997) supra).Plants are also challenged by adverse environmental conditions like coldor drought, and EREBP-like proteins appear to be involved in theresponses to these abiotic stresses as well. COR (for cold-regulated)gene expression is induced during cold acclimation, the process by whichplants increase their resistance to freezing in response to lowunfreezing temperatures. The Arabidopsis EREBP-like gene CBF1(Stockinger et al. (1997) Proc. Natl. Acad. Sci. USA 94: 1035-1040) is aregulator of the cold acclimation response, because ectopic expressionof CBF1 in Arabidopsis transgenic plants induced COR gene expression inthe absence of a cold stimulus, and the plant freezing tolerance wasincreased (Jaglo-Ottosen et al. (1998) Science 280: 104-106). Finally,another Arabidopsis EREBP-like gene, ABI4, is involved in ABA signaltransduction, because abi4 mutants are insensitive to ABA (ABA is aplant hormone that regulates many agronomically important aspects ofplant development; Finkelstein et al. (1998) Plant Cell 10: 1043-1054).

Of the sequences examined to date, two valine residues were found thatare present in members of the G47 clade but not outside of the clade(indicated by the arrows in FIG. 3). All members of the clade examinedthus far have the subsequence:

V-(X)₁₇-A-A-V-A-H-D-X-A (SEQ ID NO: 1262), where X is any amino acid andthe identified residues are indicated by the residues shown in the boxesin FIG. 3.

The SCR Family, Including the G922 Clade.

The SCARECROW gene, which regulates an asymmetric cell divisionessential for proper radial organization of root cell layers, wasisolated from Arabidopsis thaliana by screening a genomic library withsequences flanking a T-DNA insertion causing a “scarecrow” mutation (DiLaurenzio et al. (1996) Cell 86, 423-433). The gene product wastentatively described as a transcription factor based on the presence ofhomopolymeric stretches of several amino acids, the presence of a basicdomain similar to that of the basic-leucine zipper family oftranscription factors, and the presence of leucine heptad repeats. Thepresence of several Arabidopsis ESTs with gene products homologous tothe SCARECROW gene were noted. The ability of the SCARECROW gene tocomplement the scarecrow mutation was also demonstrated (Malamy et al.(1997) Plant J. 12, 957-963).

More recently, the SCARECROW homologue RGA, which encodes a negativeregulator of the gibberellin signal transduction pathway, was isolatedfrom Arabidopsis by genomic subtraction (Silverstone et al. (1998) PlantCell 10, 155-169). The RGA gene was shown to be expressed in manydifferent tissues and the RGA protein was shown to be localized to thenucleus. The same gene was isolated by Truong (Truong et al. (1997) FEBSLett. 410: 213-218) by identifying cDNA clones which complement a yeastnitrogen metabolism mutant, suggesting that RGA may be involved inregulating diverse metabolic processes. Another SCARECROW homologuedesignated GAI, which also is involved in gibberellin signalingprocesses, has been isolated by Peng (Peng et al. (1997) Genes Dev. 11,3194-3205). Interestingly, GAI is the gene that initiated the GreenRevolution. Peng et al. (Peng et al. (1999) Nature 6741, 256-261) haverecently shown that maize GAI orthologs, when mutated, result in plantsthat are shorter, have increased seed yield, and are more resistant todamage by rain and wind than wild type plants. Based on the inclusion ofthe GAI, RGA and SCR genes in this family, it has also been referred toas the GRAS family (Pysh et al. (1999) Plant J 18, 111-19).

The scarecrow gene family has 32 members in the Arabidopsis genome.

The WRKY Family, Including the G1274 Clade.

The WRKY family of transcription factors is thus far only found inplants. It is primarily characterized by a 60 amino acid conserved DNAbinding domain and a zinc finger domain. The family is divided intogroups based on whether the protein has two or only one WRKY domain(Groups I and II, respectively), and further subdivided based on aunique variation of the zing finger motif (Group III) as described byEulgem (Eulgem et al. (2000) Trends Plant Science 5:199-206). G1274(polynucleotide SEQ ID NO: 5 and polypeptide SEQ ID NO: 6) belongs tothe so-called Group II class of WRKY proteins, which can be furthersubdivided into 5 groups (a-e) based on conserved structural featuresoutside of the WRKY domain. G1274 is a member of the IIc subgroup.

The phylogenetic tree in FIG. 17 uses other closely related members ofthe WRKY Group IIc family as a natural out-group to the G1274 clade.Using either the full protein, or WRKY domain, the potentiallyorthologous sequences shown on the tree appear most closely related tothe G1274 paralog clade. FIG. 16 indicates amino acids within the WRKYdomain that differentiate the G1274 clade from the out-group. Notablefor the G1274 clade are the conserved K at position 264, the N atposition 275, the S at position 280, and the F/Y at position 299(indicated by arrows in FIG. 16). These residues are potentiallyresponsible for the conserved structure/function of this clade withregard to drought tolerance. The G1274 domain may thus be distinguishedby the subsequence:

(SEQ ID NO: 1263) RR-K-Y-G-K-K-(X)₈-R-N-Y-(X)₂-C-S-(X)₅-V-K-K-X-V-X-R-(X)₆-Y/F-V .

Amino acid residues within the WRKY domain that distinguish the G1274clade sequences, and are putatively responsible for conservedfunctionality, are indicated within the boxes in FIG. 16.

Based on full-length protein sequence, G1758 appears firmly in the G1274clade. However, FIG. 16 shows that, within the WRKY domain, G1758 isintermediate between the out-group and the claimed sequences. Theseamino acid differences may represent specific changes that retaindrought tolerance function, or possibly more finely delineate the keyresidues required for function.

The NAC Family, Including the G2053 Clade.

The NAC family is a group of transcription factors that share a highlyconserved N-terminal domain of about 150 amino acids, designated the NACdomain (NAC stands for Petunia, N A M, and Arabidopsis, ATAF1, ATAF2 andCUC2). This is believed to be a novel domain that is present in bothmonocot and dicot plants but is absent from yeast and animal proteins.One hundred and twelve members of the NAC family have been identified inthe Arabidopsis genome. The NAC class of proteins can be divided into atleast two sub-families on the basis of amino acid sequence similaritieswithin the NAC domain. One sub-family is built around the NAM and CUC2(cup-shaped cotyledon) proteins whilst the other sub-family containsfactors with a NAC domain similar to those of ATAF1 and ATAF2.

Thus far, little is known about the function of different NAC familymembers. This is surprising given that there are 113 members inArabidopsis. However, NAM, CUC1 and CUC2 are thought to have vital rolesin the regulation of embryo and flower development. In Petunia, nammutant embryos fail to develop a shoot apical meristem (SAM) and havefused cotyledons. These mutants sometimes generate escape shoots thatproduce defective flowers with extra petals and fused organs. InArabidopsis, the cuc1 and cuc2 mutations have somewhat similar effects,causing defects in SAM formation and the separation of cotyledons,sepals and stamens.

Although nam and cuc mutants exhibit comparable defects duringembryogenesis, the penetrance of these phenotypes is much lower in cucmutants. Functional redundancy of the CUC genes in Arabidopsis mayexplain this observation. In terms of the flower phenotype there arenotable differences between nam and cuc mutants. Flowers of cuc mutantsdo not contain additional organs and the formation of sepals and stamensis most strongly affected. In nam mutants, by contrast, the flowers docarry additional organs and petal formation is more markedly affectedthan that of other floral organs. These apparent differences might beexplained in two ways: the NAM and CUC proteins have been recruited intodifferent roles in development of Arabidopsis and Petunia flowers.Alternatively, the proteins could share a common function between thetwo species, with the different mutant floral phenotypes arising fromvariations in the way other genes (that participate in the samedevelopmental processes) are affected by defects in NAM or CUC.

A further gene from this family, NAP (NAC-like activated by AP3/PI) isalso involved in flower development and is thought to influence thetransition between cell division and cell expansion in stamens andpetals. Overall, then, the NAC proteins mainly appear to regulatedevelopmental processes.

The ZF-HD Family, Including the G2999 Clade.

Since their discovery in 1983, the homeobox genes (the name of whichderives from the homeotic mutations that affect Drosophila development)have been found in all eukaryotes examined, including yeast, plants, andanimals (McGinnis et al. (1984) Nature 308: 428-433; McGinnis et al.(1984) Cell 37: 403-408; Scott et al. (1984) Proc. Natl. Acad. Sci.U.S.A. 81: 4115-4119; Scott et al. (1989) Biochim. Biophys. Acta. 989,25-48; Shepherd et al. (1984) Nature 310: 70-71; Gehring et al. (1987)Science 236: 1245-1252; Vollbrecht et al. (1991) Nature 350: 241-243;Ruberti et al. (1991) EMBO J. 10: 1787-1791; and Schena and Davis (1992)Genes. Dev. 7, 367-379. The homeobox (HB) is a conserved DNA stretchthat encodes an approximate 61 amino acid region termed the homeodomain(HD). It is well demonstrated that homeodomain proteins aretranscription factors, and that the homeodomain is responsible forsequence specific recognition and binding of DNA (Affolter et al. (1990)Curr Opin Cell Biol. 2: 485-495; Hayashi and Scott (1990) Cell 63:883-894, and references therein). Genetic and structural analysisindicate that the homeodomain operates by fitting the most conserved ofthree α-helices, helix 3, directly into the major groove of the DNA(Hanes and Brent (1989) Cell 57: 1275-1283; Hanes and Brent (1991)Science 251: 426-430; Kissinger et al. (1990) Cell 63: 579-590; andWolberger et al. (1991) Cell 67: 517-528). A general review on thehomeobox genes is provided by Duboule, D. (1994). Guidebook to theHomeobox Genes. Oxford, Oxford University Press.

Homeobox genes play many important roles in the developmental processesof multicellular animals. In Drosophila, for example, a variety of thesegenes have functions in embryo development. Initially, they actmaternally to establish anterior-posterior polarity. Later, homeoboxgenes are known to regulate the segmentation process, dorso-ventraldifferentiation, and control cell fate determination in the eye andnervous system (Scott et al. (1989) supra).

A large number of homeodomain proteins have now been identified in arange of higher plants (Burglin (1997) Nucleic Acids Res. 25: 4173-4180;Burglin (1998) Dev. Genes Evol. 208: 113-116), which are herein definedas the containing the ‘classical’ type of homeodomain (FIGS. 6A-6C).These exhibit many differences to animal homeodomain proteins outsidethe conserved domain, but all contain the signature WFXNX[RK] (SEQ IDNO: 1264; X=any amino acid, [RK] indicates either an R or K residue atthis position) within the third helix. Data from the Genome Initiativeindicate that there are around 90 Arabidopsis classical homeobox genes.These are now being implicated in the control of a wide range ofdifferent processes. In many cases, plant homeodomains are found inproteins in combination with additional regulatory motifs such asleucine zippers. Classical plant homeodomain proteins can be broadlycategorized into the following different classes based on homologieswithin the family, and the presence of other types of domain: KNOX classI, KNOX class II, HD-BEL1, HD-ZIP class I, HD-ZIP class II, HD-ZIP classIII, HD-ZIP class IV (GL2 like), PHD finger type, and WUSCHEL-like(Freeling and Hake (1985); Genetics 111: 617-634 Vollbrecht et al.(1991) supra; Schindler et al. (1993) Plant J. 4:137-150; Sessa et al.(1994)). In: Puigdomenech P, Coruzzi G, (eds) Molecular genetic analysisof plant development and metabolism, pp. 411-426. Springer Verlag,Berlin; Kerstetter et al. (1994) Plant Cell 6: 1877-1887; Kerstetter etal. (1997) Development 124: 3045-3054; Burglin (1997) supra; Burglin(1998) supra; Schoof et al. (2000) Cell 100: 635-644).

Recently a novel class of proteins was discovered that contain a domainsimilar to the classical homeodomain, in combination with N-terminalzinc finger motifs, by Windhovel (Windhovel et al. (2001) Plant Mol.Biol. 45: 201-214), while studying the regulatory mechanisms responsiblefor the mesophyll specific expression of the C4 phosphoenolpyruvate geneof Flavaria trinervia. Using a yeast one-hybrid screen, these workersrecovered five cDNA clones, which encoded proteins that were capable ofspecifically binding the promoter of the Flavaria C4 phosphoenolpyruvategene, but not the promoter of a Flavaria C3 phosphoenolpyruvate gene.One-hybrid experiments and in vitro DNA binding studies were then usedto confirm that these proteins specifically interact with the proximalregion of the C4 phosphoenolpyruvate gene. Four of five clones [FtHB1(GenBank accession Y18577), FbHB2 (GenBank accession Y18579), FbHB3(GenBank accession Y18580), and FbHB4 (GenBank accession Y18581), (thefifth clone encoded a histone)] all encoded a novel type of protein thatcontained two types of highly conserved domains. At the C-termini, aregion was apparent that had many of the features of a homeodomain,whereas at the N-termini, two putative zinc finger motifs were present.Yeast two-hybrid experiments were used to show that the zinc fingermotifs are sufficient to confer homo and hetero-dimerization between theproteins, and mutagenesis experiments demonstrated that conservedcysteine residues within the motifs are essential for such dimerization.Given the presence of the potential homeodomain and zinc fingers,Windhovel (Windhovel et al. (2001) supra) named this new class ofproteins as the ZF-HD group.

That four proteins of this type were identified in the above studiessuggested that the family might have a specific role in establishingexpression of the C4 phosphoenolpyruvate gene within mesophyll cells.However, database searches revealed that proteins of this class are alsopresent in C3 species, indicating that they likely have additional rolesoutside of C4 photosynthesis (Windhovel et al. (2001) supra). Inparticular, the Arabidopsis genome encodes fourteen proteins of thistype, but the functional analysis of these proteins has yet to bepublicly reported.

Secondary structure analyses performed by Windhovel (Windhovel et al.(2001) supra) indicated that the putative homeodomains of the ZF-HDproteins contain three α-helices similar to those recognized in theclasses of homeodomain already found in plants (Duboule (1994) supra).Interestingly, though, if full-length proteins of the ZF-HD group areblasted against databases, they do not preferentially align with theknown classes of plant homeodomain proteins. Furthermore, a phylogenetictree based on comparing the classical versus ZF-HD type homeodomainsreveal that the latter occupy a distinct node of the tree (FIG. 8).

A careful examination of the ZF-HD proteins reveals a particularstriking difference to the classical plant homeodomain. All of the 90 orso previously recognized plant homeodomain proteins contain thesignature WFXNX[RK] (SEQ ID NO: 1264; X=any amino acid) within the thirdhelix. However, the ZF-HD proteins all lack the invariant F residue inthis motif and generally contain an M in its place. This structuraldistinction, combined with the presence of ZF motifs in other regions ofthe protein, could confer functional properties on ZF-HD proteins thatare different to those found in other HD containing proteins.

Residues that may be used to identify the G2999 clade are shown in boxesin FIGS. 6A and 6B. As shown in FIGS. 6A and 6B, a number of amino acidresidues may be used to identify G2999 clade members. Of the G2999 clademembers examined to date, each is a ZF-HD polypeptide and comprises theconsensus subsequence:

K-(X)₁₇-W-(X)₁₃₋₁₅-C-(X)₁₂-W-(X)₂-N-N/H-K (SEQ ID NO: 1265, 1266 or1267), where X is any amino acid.

The HLH/MYC Family, Including the G3086 Clade.

The bHLH protein family is a group of transcription factors found inmammals and plants. The typical feature of this family of transcriptionfactors is that they share a highly conserved approximately 50 aminoacid DNA-binding domain. This domain consists of a basic region of 14amino acids followed by a first helix, a loop region of seven aminoacids and a second helix (Littlewood et al. (1994) Prot. Profile 1:639-709). In plants, members of this family also share, besides the bHLHdomain, a highly conserved 200 amino acid N-terminal domain. Functionalanalysis revealed that small deletions in the N-terminal domaininactivate the B protein, a member of bHLH protein family, in Z. mays(Goff et al. (1992) Genes Dev. 6: 864-875). It has also been shown thatthe N-terminal domain can interact with one of other transcriptionfactors (Myb proteins) to regulate anthocyanin biosynthesis in Z. mays(Goff et al. (1992) supra).

In mammalian systems, members of this family have been shown to controldevelopment and differentiation of a variety of cell types. The bHLHproteins play essential roles in neurogenesis or neural development, andmyogenesis (Littlewood et al. (1994) supra).

Plant bHLH proteins have been shown to play an important role in theregulation of anthocyanin biosynthesis, in the control of trichomedevelopment, in phytochrome signaling transduction pathway, and in theregulation of dehydration- and ABA-inducible gene expression. It hassuggested that the R locus of maize is responsible for determining thetemporal and spatial pattern of anthocyanin pigmentation in the plant.The R gene family consists of B, S, and Lc genes, which encode atranscription factor of the basic helix-loop-helix class (Goff et al.(1992) supra, Ludwig (1990) Cell 62: 849-851). A gene encoding a basichelix-loop-helix protein has been cloned as a phytochrome-interactingfactor in a genetic screen for T-DNA-tagged Arabidopsis mutants as wellas in a yeast two-hybrid screen. The protein functions as apositively-acting signaling intermediate (Halliday et al. (1999) Proc.Natl. Acad. Sci. USA. 96:5832-5837, Ni et al. (1998) Cell 95: 657-667).A new mutant, hfr1 (long hypocotyl in far-red) has been isolated fromQuail's lab. The hfr1 mutant exhibits a reduction in seedlingresponsiveness specifically to continuous far-red light (FRc), therebysuggesting a locus likely to be involved in phytochrome A (phyA) signaltransduction. HFR1 encodes a nuclear protein with strong similarity tothe bHLH family of DNA-binding proteins but with an atypical basicregion. In contrast to PIF3, a related bHLH protein previously shown tobind phyB, HFR1 did not bind either phyA or B. However, HFR1 did bindPIF3, suggesting heterodimerization, and both the HFR1/PIF3 complex andPIF3 homodimer bound preferentially to the Pfr form of bothphytochromes. Thus, HFR1 may function to modulate phyA signaling viaheterodimerization with PIF3. HFR1 mRNA is 30-fold more abundant in FRcthan in continuous red light, suggesting a potential mechanistic basisfor the specificity of HFR1 to phyA signaling.

The rd22BP1 protein of Arabidopsis has a typical DNA-binding domain of abasic region helix-loop-helix motif. It has been shown thattranscription of the rd22BP1 gene is induced by dehydration stress andphytohormone ABA treatment, and its induction precedes that of rd22, adehydration-responsive gene (Abe et al. (1997) Plant Cell 9: 1859-1868).

Plant bHLH proteins may also play a crucial role in the process ofnitrogen fixation, probably not acting as a transcription factor. Aprotein with a helix-loop-helix motif was identified as a symbioticammonium transport protein by functional complementation of the yeastNH₄₊ transport mutant with a soybean nodule cDNA (Kaiser et al. (1998)Science 1998 281: 1202-1206). Using similar complementation approach ofthe yeast fet3fet4 mutant strain, an iron transport protein was isolatedfrom an iron-deficient maize root cDNA expression library. The proteinhad 44% identity with an Arabidopsis bHLH-like protein RAP1 that bindsthe G-box sequence via a basic region helix-loop-helix (Loulergue (1998)Gene 225:47-57).

Another bHLH gene has been recently identified as ind1 (Liljegren et al.(2000) in 11th International Conference on Arabidopsis Research,Madison, Wis.; TAIR Accession Publication No. 1547039). They found thatfruit from a knockout mutant do not show dehiscence zonedifferentiation. In addition, their results suggest that ind1 maymediate cell differentiation during Arabidopsis fruit development. Acytokinin-repressed gene CRR12 with a basic region/helix-loop-helixmotif was identified from a cucumber cotyledon cDNA library. It wasfound that the level of CRR12 transcripts decreased in response toeither cytokinins or light in etiolated cotyledons. The mRNA was low incotyledons and leaves of light-grown plants, but it increased duringdark incubation.

As shown in FIG. 12, a number of amino acid residues may be used toidentify G3086 clade members. Of the G3086 clade members examined todate, each of their sequences comprise the consensus subsequence:

K-(X)₅-H-X-R-S-I-A-X-R-X-R-R-T-R/K-I-(X)₆-L-(X)₂-L-X-P-(X)₂-D-K-Q-T-(X)₄₋₅-M-(X)₈-K-X-L-Q(SEQ ID NOs: 1268 or 1269), where X is any amino acid.

Table 1 shows exemplary sequences of the invention that, in many cases,confer drought tolerance when overexpressed. The polypeptides areidentified by polypeptide SEQ ID NO and Identifier (for example, Gene ID(GID) No., accession number or other name), presented in order ofsimilarity to the first Arabidopsis sequence listed for each set, andincludes the conserved domains of the polypeptide in amino acidcoordinates, the respective domain sequences, and the extent of identityin percentage terms to the first Arabidopsis sequence listed for eachset.

TABLE 1Gene families and binding domains for exemplary sequences conferring droughttolerance, including paralogs and orthologs Conserved ConservedDomains in Domains in SEQ ID SEQ Polypeptide Polypeptide NO: of % ID inID Amino Acid Base Conserved conserved conserved NO: GID SpeciesCoordinates Coordinates Domain Sequence domain domain % to G2133  12G2133 Arabidopsis AP2: 10-77 AP2: 53-256 DQSKYKGIRRRKWGKW 1270 100%thaliana VSEIRVPGTRQRLWLGSF STAEGAAVAHDVAFYCL HRPSSLDDESFNFPHLL  94G3646 Brassica AP2: 10-77 AP2: 203-406 HQAKYKGIRRRKWGKW 1271  91%oleracea VSEIRVPATRERLWLGSF STAEGAAVAHDVAFYCL HRPSSLDNEAFNFPHLL  92G3645 Brassica rapa AP2: 10-75 AP2: 40-237 TQSKYKGIRRRKWGKW 1272  89%subsp. VSEIRVPGTRDRLWLGSF Pekinensis STAEGAAVAHDVAFYCL HQPNSLESLNFPHLL  2 G47 Arabidopsis AP2: 10-75 AP2: 65-262 SQSKYKGIRRRKWGKWV 1273  88%thaliana SEIRVPGTRDRLWLGSFS TAEGAAVAHDVAFFCLH QPDSLESLNFPHLL  88 G3643Glycine max AP2: 13-78 AP2: 101-298 TNNKLKGVRRRKWGKW 1274  69%VSEIRVPGTQERLWLGTY ATPEAAAVAHDVAVYCL SRPSSLDKLNFPETL  96 G3647 ZinniaAP2: 13-78 AP2: 53-250 SQKTYKGVRCRRWGKW 1275  63% elegansVSEIRVPGSRERLWLGTY STPEGAAVAHDVASYCL KGNTSFHKLNIPSML  90 G3644Oryza sativa AP2: 52-122 AP2: 154-366 ERCRYRGVRRRRWGKW 1276  54%(japonica VSEIRVPGTRERLWLGSY cultivar- ATPEAAAVAHDTAVYFL group)RGGAGDGGGGGATLNFP ERA  98 G3649 Oryza sativa AP2: 15-87 AP2: 43-261EMMRYRGVRRRRWGK 1277  53% (japonica WVSEIRVPGTRERLWLGS cultivar-YATAEAAAVAHDAAVC group) LLRLGGGRRAAAGGGGG LNFPARA 100 G3651 Oryza sativaAP2: 60-130 AP2: 178-390 ERCRYRGVRRRRWGKW 1278  52% (japonicaVSEIRVPGTRERLWLGSY cultivar- ATPEAAAVAHDTAVYFL group) RGGAGDGGGGGATAQLPGAR %ID to G922   4 G922 Arabidopsis 1st SCR: 134- 1st SCR: 400-RRLFFEMFPILKVSYLLT 1279 100% thaliana 199 597 NRAILEAMEGEKMVHVIDLDASEPAQWLALLQAF NSRPEGPPHLRITG   4 G922 Arabidopsis 2nd SCR:2nd SCR: 994- FLNAIWGLSPKVMVVTE 1280 100% thaliana 332-401 1203QDSDHNGSTLMERLLESL YTYAALFDCLETKVPRTS QDRIKVEKMLFGEEIKN   4 G922Arabidopsis 3rd SCR: 405- 3rd SCR: 1213- CEGEERRERHEKLEKWS 1281 100%thaliana 478 1434 QRIDLAGFGNVPLSYYA MLQARRLLQGCGFDGYR IKEESGCAVICWQDRPLYSVSAW 220 G3824 Lycopersicon 1st SCR: 42- 1st SCR: 134-RKMFFEIFPFLKVAFVVT 1282  69% esculentum 107 331 NQAIIEAMEGEKMVHIVDLNAAEPLQWRALLQDLS ARPEGPPHLRITG 220 G3824 Lycopersicon 2nd SCR:2nd SCR: 713- FLNALWGLSPKVMVVTE 1283  78% esculentum 235-304 922QDANHNGTTLMERLSES LHFYAALFDCLESTLPRT SLERLKVEKMLLGEEIRN 220 G3824Lycopersicon 3rd SCR: 308- 3rd SCR: 932- CEGIERKERHEKLEKWFQ 1284  77%esculentum 381 1153 RFDTSGFGNVPLSYYAM LQARRLLQSYSCEGYKIKEDNGCVVICWQDRPLFS VSSW 212 G3810 Glycine max 1st SCR: 106- 1st SCR: 316-QKLFFELFPFLKVAFVLT 1285  68% 171 513 NQAIIEAMEGEKVIHIIDLNAAEAAQWIALLRVLSA HPEGPPHLRITG 212 G3810 Glycine max 2nd SCR:2nd SCR: 913- FLNALWGLSPKVMVVTE 1286  80% 305-374 1122 QDCNHNGPTLMDRLLEALYSYAALFDCLESTVSRT SLERLRVEKMLFGEEIKN 212 G3810 Glycine max3rd SCR: 378- 3rd SCR: 1132- CEGSERKERHEKLEKWF 1287  71% 451 1353QRFDLAGFGNVPLSYFG MVQARRFLQSYGCEGYR MRDENGCVLICWEDRPM YSISAW 214 G3811Glycine max 1st SCR: 103- 1st SCR: 361- QKLFFELLPFLKESYILTN 1288  68%168 558 QAIVEAMEGEKMVHIVD LYGAGPAQWISLLQVLS ARPEGPPHLRITG 214 G3811Glycine max 2nd SCR: 2nd SCR: 940- FLNALWGLSPKVMVVTE 1289  74% 296-3651149 QDFNHNCLTMMERLAEA LFSYAAYFDCLESTVSRA SMDRLKLEKMLFGEEIK N 214 G3811Glycine max 3rd SCR: 369- 3rd SCR: 1159- CEGCERKERHEKMDRWI 1290  60% 4421380 QRLDLSGFANVPISYYGM LQGRRFLQTYGCEGYKM REECGRVMICWQERSLFS ITAW 218G3814 Oryza sativa 1st SCR: 123- 1st SCR: 367- RRHMFDVLPFLKLAYLT 1291 60% (japonica 190 570 TNHAILEAMEGERFVHV cultivar- VDFSGPAANPVQWIALFgroup) HAFRGRREGPPHLRITA 218 G3814 Oryza sativa 2nd SCR: 2nd SCR: 994-FLSAVRSLSPKIMVMTEQ 1292  48% (japonica 332-400 1200 EANHNGGAFQERFDEALcultivar- NYYASLFDCLQRSAAAA group) AERARVERVLLGEEIRG 218 G3814Oryza sativa 3rd SCR: 404- 3rd SCR: 1210- CEGAERVERHERARQWA 1293  46%(japonica 480 1440 ARMEAAGMERVGLSYSG cultivar- AMEARKLLQSCGWAGP group)YEVRHDAGGHGFFFCWH KRPLYAVTAW 216 G3813 Oryza sativa 1st SCR: 129-1st SCR: 385- RRHFLDLCPFLRLAGAAA 1294  53% (japonica 194 582NQSILEAMESEKIVHVIDL cultivar- GGADATQWLELLHLLAA group) RPEGPPHLRLTS 216G3813 Oryza sativa 2nd SCR: 2nd SCR: 868- FLGALWGLSPKVMVVAE 1295  61%(japonica 290-359 1077 QEASHNAAGLTERFVEA cultivar- LNYYAALFDCLEVGAARgroup) GSVERARVERWLLGEEIK N 216 G3813 Oryza sativa 3rd SCR: 363-3rd SCR: 1087- CDGGERRERHERLERWA 1296  64% (japonica 436 1308RRLEGAGFGRVPLSYYA cultivar- LLQARRVAQGLGCDGFK group) VREEKGNFFLCWQDRALFSVSAW 222 G3827 Oryza sativa 2nd SCR: 2nd SCR: 676- DVESLRGLSLKVMVVTE1297  55% (japonica 226-295 885 QEVSHNAAGLTERFVEA cultivar-LNYYAALFDCLEVGGAR group) GSVERTRVERWLLGEEIK N 222 G3827 Oryza sativa3rd SCR: 299- 3rd SCR: 895- CDGGERRERHERLEGAG 1298  60% (japonica 3651095 FGRVPLSYYALLQARRV cultivar- AQGLGCDGFKVREEKGN group)FFLCWQDRALFSVSAW %ID to G1274   6 G1274 Arabidopsis WRKY: 110-WRKY: 328- DDGFKWRKYGKKSVKN 1299 100% thaliana 166 498NINKRNYYKCSSEGCSVK KRVERDGDDAAYVITTY EGVHNH 140 G3724 Glycine maxWRKY:107- WRKY: 390- DDGYKWRKYGKKSVKS 1300  84% 163 560SPNLRNYYKCSSGGCSV KKRVERDRDDYSYVITT YEGVHNH 148 G3728 Zea maysWRKY: 108- WRKY: 1075- DDGFKWRKYGKKAVKN 1301  82% 164 1245SPNPRNYYRCSSEGCGVK KRVERDRDDPRYVITTY DGVHNH 206 G3802 Sorghum WRKY: 110-WRKY: 386- DDGFKWRKYGKKAVKN 1302  82% bicolor 166 556 SPNPRNYYRCSSEGCGVKKRVERDRDDPRYVITTY DGVHNH 210 G3804 Zea mays WRKY: 108- WRKY: 438-DDGFKWRKYGKKAVKN 1303  82% 164 608 SPNPRNYYRCSSEGCGVK KRVERDRDDPRYVITTYDGVHNH 146 G3727 Zea mays WRKY: 102- WRKY: 391- DDGFKWRKYGKKAVKS 1304 80% 158 561 SPNPRNYYRCSSEGCGVK KRVERDRDDPRYVITTY DGVHNH 154 G3731Lycopersicon WRKY: 95- WRKY: 297- DDGFKCRKYGKKMVKN 1305  80% esculentum151 467 NPNPRNYYKCSSGGCNV KKRVERDNKDSSYVITTY EGIHNH 156 G3732 SolanumWRKY: 95- WRKY: 309- DDGFKWRKYGKKMVKN 1306  80% tuberosum 151 479SSNPRNYYKCSSGGCNV KKRVERDNEDSSYVITTY EGIHNH 158 G3733 Hordeum WRKY: 131-WRKY: 641- DDGYKWRKYGKKSVKN 1307  80% vulgare 187 811 SPNPRNYYRCSTEGCSVKKRVERDRDDPAYVVTTY EGTHSH 204 G3797 Lactuca WRKY: 118- WRKY: 363-DDGFKWRKYGKKMVKN 1308  80% sativa 174 533 SPNPRNYYRCSAAGCSVKKRVERDVEDARYVITT YEGIHNH 208 G3803 Glycine max WRKY: 111- WRKY: 367-DDGYKWRKYGKKTVKN 1309  80% 167 537 NPNPRNYYKCSGEGCNV KKRVERDRDDSNYVLTTYDGVHNH 132 G3720 Zea mays WRKY: 135- WRKY: 403- DDGYKWRKYGKKSVKN 1310 78% 191 573 SPNPRNYYRCSTEGCNV KKRVERDKDDPSYVVTT YEGMHNH 134 G3721Oryza sativa WRKY: 96- WRKY: 342- DDGFKWRKYGKKAVKN 1311  78% (japonica152 512 SPNPRNYYRCSTEGCNV cultivar- KKRVERDREDHRYVITT group) YDGVHNH 136G3722 Zea mays WRKY: 129- WRKY: 430- DDGYKWRKYGKKSVKN 1312  78% 185 600SPNPRNYYRCSTEGCNV KKRVERDRDDPRYVVTM YEGVHNH 144 G3726 Oryza sativaWRKY: 135- WRKY: 459- DDGYKWRKYGKKSVKN 1313  78% (japonica 191 629SPNPRNYYRCSTEGCNV cultivar- KKRVERDKDDPSYVVTT group) YEGTHNH 202 G3795Capsicum WRKY: 95- WRKY: 302- DDGYKWRKYGKKMVK 1314  78% annuum 151 472NSPNPRNYYRCSVEGCPV KKRVERDKEDSRYVITTY EGVHNH  30 G1275 ArabidopsisWRKY: 113- WRKY: 394- DDGFKWRKYGKKMVKN 1315  77% thaliana 169 564SPHPRNYYKCSVDGCPV KKRVERDRDDPSFVITTY EGSHNH 138 G3723 Glycine maxWRKY: 113- WRKY: 715- DDGYKWRKYGKKTVKS 1316  77% 169 885SPNPRNYYKCSGEGCDV KKRVERDRDDSNYVLTT YDGVHNH 152 G3730 Oryza sativaWRKY: 107- WRKY: 385- DDGFKWRKYGKKAVKS 1317  77% (japonica 163 555SPNPRNYYRCSAAGCGV cultivar- KKRVERDGDDPRYVVTT group) YDGVHNH 130 G3719Zea mays WRKY: 91- WRKY: 428- DDGFKWRKYGKKAVKS 1318  75% 147 598SPNPRNYYRCSTEGSGVK KRVERDSDDPRYVVTTY DGVHNH 142 G3725 Oryza sativaWRKY: 158- WRKY: 688- DDGYKWRKYGKKSVKN 1319  75% (japonica 214 858SPNPRNYYRCSTEGCNV cultivar- KKRVERDKNDPRYVVT group) MYEGIHNH 150 G3729Oryza sativa WRKY: 137- WRKY: 452- DDGYRWRKYGKKMVKN 1320  75% (japonica193 622 SPNPRNYYRCSSEGCRVK cultivar- KRVERARDDARFVVTTY group) DGVHNH  32G1758 Arabidopsis WRKY: 109- WRKY: 393- DDGYKWRKYGKKPITGS 1321  57%thaliana 165 563 PFPRHYHKCSSPDCNVKK KIERDTNNPDYILTTYEG RHNH %ID to G1792  8 G1792 Arabidopsis AP2: 16-80 AP2: 122-316 KQARFRGVRRRPWGKFA 1322100% thaliana AEIRDPSRNGARLWLGTF ETAEEAARAYDRAAFNL RGHLAILNFPNEY  86G3520 Glycine max AP2: 14-78 AP2: 50-244 EEPRYRGVRRRPWGKFA 1323  80%AEIRDPARHGARVWLGT FLTAEEAARAYDRAAYE MRGALAVLNFPNEY  82 G3518 Glycine maxAP2: 13-77 AP2: 134-328 VEVRYRGIRRRPWGKFA 1324  76% AEIRDPTRKGTRIWLGTFDTAEQAARAYDAAAFHF RGHRAILNFPNEY  84 G3519 Glycine max AP2: 13-77AP2: 93-287 CEVRYRGIRRRPWGKFA 1325  76% AEIRDPTRKGTRIWLGTFDTAEQAARAYDAAAFHF RGHRAILNFPNEY 160 G3735 Medicago AP2: 23-87AP2: 148-342 DQIKYRGIRRRPWGKFA 1326  76% truncatula AEIRDPTRKGTRIWLGTFDTAEQAARAYDAAAFHF RGHRAILNFPNEY  34 G1791 Arabidopsis AP2: 10-74AP2: 63-257 NEMKYRGVRKRPWGKY 1327  72% thaliana AAEIRDSARHGARVWLGTFNTAEDAARAYDRAAF GMRGQRAILNFPHEY  70 G3380 Oryza sativa AP2: 18-82AP2: 138-332 ETTKYRGVRRRPSGKFA 1328  72% (japonica AEIRDSSRQSVRVWLGTFcultivar- DTAEEAARAYDRAAYA group) MRGHLAVLNFPAEA  74 G3383 Oryza sativaAP2: 9-73 AP2: 25-219 TATKYRGVRRRPWGKFA 1329  72% (japonicaAEIRDPERGGARVWLGT cultivar- FDTAEEAARAYDRAAYA group) QRGAAAVLNFPAAA  18G30 Arabidopsis AP2: 16-80 AP2: 86-280 EQGKYRGVRRRPWGKY 1330  70%thaliana AAEIRDSRKHGERVWLG TFDTAEDAARAYDRAAY SMRGKAAILNFPHEY  72 G3381Oryza sativa AP2: 14-78 AP2: 122-316 LVAKYRGVRRRPWGKFA 1331  70%(japonica AEIRDSSRHGVRVWLGTF cultivar- DTAEEAARAYDRSAYSM group)RGANAVLNFPADA  76 G3515 Oryza sativa AP2: 11-75 AP2: 53-247SSSSYRGVRKRPWGKFA 1332  70% (japonica AEIRDPERGGARVWLGT cultivar-FDTAEEAARAYDRAAFA group) MKGATAMLNFPGDH  78 G3516 Zea mays AP2: 6-70AP2: 16-210 KEGKYRGVRKRPWGKF 1333  70% AAEIRDPERGGSRVWLGTFDTAEEAARAYDRAAF AMKGATAVLNFPASG 164 G3737 Oryza sativa AP2: 8-72AP2: 233-427 AASKYRGVRRRPWGKFA 1334  70% (japonica AEIRDPERGGSRVWLGTFcultivar- DTAEEAARAYDRAAFAM group) KGAMAVLNFPGRT  36 G1795 ArabidopsisAP2: 11-75 AP2: 57-251 EHGKYRGVRRRPWGKY 1335  69% thalianaAAEIRDSRKHGERVWLG TFDTAEEAARAYDQAAY SMRGQAAILNFPHEY 200 G3794 Zea maysAP2: 6-70 AP2: 135-329 EPTKYRGVRRRPSGKFA 1336  69% AEIRDSSRQSVRMVVLGTFDTAEEAARAYDRAAYA MRGQIAVLNFPAEA  80 G3517 Zea mays AP2: 13-77AP2: 76-270 EPTKYRGVRRRPWGKYA 1337  67% AEIRDSSRHGVRIWLGTFDTAEEAARAYDRSANSM RGANAVLNFPEDA 162 G3736 Triticum AP2: 12-76AP2: 163-357 EPTKYRGVRRRPWGKFA 1338  67% aestivum AEIRDSSRHGVRMWLGTFDTAEEAAAAYDRSAYS MRGRNAVLNFPDRA 166 G3739 Zea mays AP2: 13-77AP2: 211-405 EPTKYRGVRRRPWGKYA 1339  67% AEIRDSSRHGVRIWLGTFDTAEEAARAYDRSAYSM RGANAVLNFPEDA %ID to G2053  10 G2053 ArabidopsisNAC: 6-152 NAC: 16-456 GLRFRPTDKEIVVDYLRP 1340 100% thalianaKNSDRDTSHVDRVISTVT IRSFDPWELPCQSRIKLKD ESWCFFSPKENKYGRGDQQIRKTKSGYWKITGKPK PILRNRQEIGEKKVLMFY MSKELGGSKSDWVMHE YHAFSPTQMMMTYTICKVMFKGD  20 G515 Arabidopsis NAC: 6-149 NAC: 93-524 GLRFCPTDEEIVVDYLWP1341  78% thaliana KNSDRDTSHVDRFINTVP VCRLDPWELPCQSRIKLKDVAWCFFRPKENKYGRG DQQMRKTKSGFWKSTGR PKPIMRNRQQIGEKKILMFYTSKESKSDWVIHEYHG FSHNQMMMTYTLCKVM FNGG  24 G517 Arabidopsis NAC: 6-153NAC: 16-459 GFRFRPNDEEIVDHYLRP 1342  62% thaliana KNLDSDTSHVDEVISTVDICSFEPWDLPSKSMIKSRD GVWYFFSVKEMKYNRG DQQRRRTNSGFWKKTGK TMTVMRKRGNREKIGEKRVLVFKNRDGSKTDWV MHEYHATSLFPNQMMTY TVCKVEFKGE  22 G516 ArabidopsisNAC: 6-141 NAC: 16-423 GFRFRPTDGEIVDIYLRPK 1343  55% thalianaNLESNTSHVDEVISTVDIC SFDPWDLPSHSRMKTRD QVWYFFGRKENKYGKG DRQIRKTKSGFWKKTGVTMDIMRKTGDREKIGEK RVLVFKNHGGSKSDWA MHEYHATFSSPNQGE %ID to G2999  14G2999 Arabidopsis ZF: 80-133 ZF: 280-441 ARYRECQKNHAASSGGH 1344 100%thaliana VVDGCGEFMSSGEEGTV ESLLCAACDCHRSFERKE ID  14 G2999 ArabidopsisHB: 198-261 HB: 634-825 KKRFRTKFNEEQKEKMM 1345 100% thalianaEFAEKIGWRMTKLEDDE VNRFCREIKVKRQVFKV WMHNNKQAAKKKD  62 G2998 ArabidopsisZF: 74-127 ZF: 220-381 VRYRECLKNHAASVGGS 1346  79% thalianaVHDGCGEFMPSGEEGTIE ALRCAACDCHRNFERKE MD  62 G2998 ArabidopsisHB: 240-303 HB: 718-909 KKRFRTKFTTDQKERMM 1347  78% thalianaDFAEKLGWRMNKQDEE ELKRFCGEIGVKRQVFKV WMHNNKNNAKKPP  64 G3000 ArabidopsisZF: 58-111 ZF: 318-479 AKYRECQKNHAASTGGH 1348  77% thalianaVVDGCCEFMAGGEEGTL GALKCAACNCHRSFHRK EVY  64 G3000 ArabidopsisHB: 181-244 HB: 687-878 KKRVRTKINEEQKEKMK 1349  65% thalianaEFAERLGWRMQKKDEEE IDKFCRMVNLRRQVFKV WMHNNKQAMKRNN 106 G3670 LotusZF: 62-115 ZF: 184-345 VRYRECQKNHAVSEGGH 1350  74% corniculatusAVDGCCEFMAAGDEGTL var. EAVICAACNCHRNFHRK japonicus EID 106 G3670 LotusHB: 207-270 HB: 619-810 KKRYRTKFTPEQKEKML 1351  57% corniculatusAFAEELGWRIQKHQEAA var. VEQFCAETCVRRNVLKV japonicus WMHNNKNTLGKKP 110G3674 Oryza sativa ZF: 61-114 ZF: 274-435 ARYRECLKNHAVGIGGH 1352  72%(indica AVDGCGEFMASGEEGSI cultivar- DALRCAACGCHRNFHRK group) ESE 110G3674 Oryza sativa HB: 226-289 HB: 769-960 KKRFRTKFTQEQKDKML 1353  59%(indica AFAERLGWRIQKHDEAA cultivar- VQQFCEEVCVKRHVLKV group)WMHNNKHTLGKKA 102 G3663 Lotus ZF: 88-141 ZF: 262-423 IRYRECLRNHAARLGSHV1354  70% corniculatus TDGCGEFMPNGEQGTPE var. SLICAACECHRNFERKEAjaponicus Q 102 G3663 Lotus HB: 219-282 HB: 655-846 KKRFRTKFTQQQKDRM1355  64% corniculatus MEFAEKLGWKIQKQDEE var. EVKQFCSHVGVKRQAFKjaponicus VWMHNSKQAMKKKQ 108 G3671 Oryza sativa ZF: 40-93 ZF: 233-394GRYRECLKNHAVGIGGH 1356  70% (japonica AVDGCGEFMAAGEEGTI cultivar-DALRCAACNCHRNFHRK group) ESE 108 G3671 Oryza sativa HB: 200-263HB: 713-904 KKRFRTKFTQEQKDKML 1357  59% (japonica AFAERVGWRIQKHDEAAcultivar- VQQFCDEVGVKRHVLKV group) WMHNNKHTLGKKL  60 G2997 ArabidopsisZF: 47-100 ZF: 263-424 IRYRECLKNHAVNIGGHA 1358  68% thalianaVDGCCEFMPSGEDGTLD ALKCAACGCHRNFHRKE TE  60 G2997 Arabidopsis HB: 157-220HB: 593-784 TKRFRTKFTAEQKEKML 1359  59% thaliana AFAERLGWRIQKHDDVAVEQFCAETGVRRQVLKI WMHNNKNSLGKKP 116 G3683 Oryza sativa ZF: 72-125ZF: 214-375 ARYRECLKNHAAAIGGS 1360  68% (japonica ATDGCGEFMPGGEEGSLcultivar- DALRCSACGCHRNFHRK group) ELD 116 G3683 Oryza sativaHB: 193-256 HB: 577-768 RKRERTKFTAEQKARML 1361  59% (japonicaGFAEEVGWRLQKLEDAV cultivar- VQRFCQEVGVKRRVLKV group) WMHNNKHTLARRH 112G3675 Brassica ZF: 49-102 ZF: 201-362 VRYRECLKNHAVNIGGH 1362  66% napusAVDGCCEFMPSGEDGSL DALKCAACGCHRNFHRK ETE 112 G3675 Brassica HB: 162-225HB: 540-731 AKRFRTKFTAEQKDKML 1363  56% napus AFAERLGWRIQKHDDAAVEQFCAETGVRRQVLKI WMHNNKNSLGRKP 122 G3690 Oryza sativa ZF: 161-213ZF: 481-639 WRYRECLKNHAARMGA 1364  66% (japonica HVLDGCGEFMSSPGDGAcultivar- AALACAACGCHRSFHRR group) EPA 122 G3690 Oryza sativaHB: 318-381 HB: 952-1143 KKRERTKFTAEQKERIVIR 1365  56% (japonicaEFAHRVGWRIHKPDAAA cultivar- VDAFCAQVGVSRRVLKV group) WMHNNKHLAKTPP 104G3668 Flaveria ZF: 42-95 ZF: 410-571 YRYKECLKNHAVGIGGQ 1366  64%bidentis AVDGCGEFMAAGDEGTL DALKCAACNCHRNFHRK EVE 104 G3668 FlaveriaHB: 174-237 HB: 806-997 KKRFRTKFTQDQKDRML 1367  54% bidentisAFSEALGWRIQKHDEAA VQQFCNETGVKRHVLKV WMHNNKHTIGKKP  58 G2996 ArabidopsisZF: 73-126 ZF: 241-402 FRFRECLKNQAVNIGGH 1368  64% thalianaAVDGCGEFMPAGIEGTID ALKCAACGCHRNFHRKE LP  58 G2996 ArabidopsisHB: 191-254 HB: 595-786 RKRHRTKFTAEQKERML 1369  53% thalianaALAERIGWRIQRQDDEVI QRFCQETGVPRQVLKVW LHNNKHTLGKSP  54 G2994 ArabidopsisZF: 88-141 ZF: 329-490 IKYKECLKNHAAAMGGN 1370  62% thalianaATDGCGEFMPSGEDGSIE ALTCSACNCHRNFHRKE VE  54 G2994 ArabidopsisHB: 218-281 HB: 719-910 KKRFRTKFTPEQKEKMLS 1371  65% thalianaFAEKVGWKIQRQEDCVV QRFCEEIGVKRRVLKVW MHNNKIHFSKKN 120 G3686 Oryza sativaZF: 38-88 ZF: 112-264 CRYHECLRNHAAASGGH 1372  62% (indicaVVDGCGEFMPASFEEPL cultivar- ACAACGCHRSFHRRDPS group) 120 G3686Oryza sativa HB: 159-222 HB: 475-666 RRRSRTTFTREQKEQML 1373  50% (indicaAFAERVGWRIQRQEEAT cultivar- VEHFCAQVGVRRQALKV group) WMHNNKHSFKQKQ  52G2993 Arabidopsis ZF: 85-138 ZF: 442-603 IKYKECLKNHAATMGGN 1374  61%thaliana AIDGCGEFMPSGEEGSIE ALTCSVCNCHRNFHRRE IL  52 G2993 ArabidopsisHB: 222-285 HB: 853-1044 KKRFRTKFTQEQKEKMIS 1375  57% thalianaFAERVGWKIQRQEESVV QQLCQEIGIRRRVLKVW MHNNKQNLSKKS  48 G2991 ArabidopsisZF: 54-109 ZF: 218-385 ATYKECLKNHAAGIGGH 1376  60% thalianaALDGCGEFMPSPSFNSND PASLTCAACGCHRNFHR REED  48 G2991 ArabidopsisHB: 179-242 HB: 593-784 RKRFRTKFSQYQKEKMF 1377  59% thalianaEFSERVGWRMPKADDVV VKEFCREIGVDKSVFKV WMHNNKISGRSGA 114 G3680 Zea maysZF: 34-89 ZF: 223-390 PLYRECLKNHAASLGGH 1378  60% AVDGCGEFMPSPGANPADPTSLKCAACGCHRNFH RRTLE 114 G3680 Zea mays HB: 222-285 HB: 787-978RKRFRTKFTAEQKQRMQ 1379  50% ELSERLGWRLQKRDEAIV DEWCRDIGVGKGVFKVWMHNNKHNFLGGH 118 G3685 Oryza sativa ZF: 43-95 ZF: 216-374VRYHECLRNHAAAMGG 1380  59% (japonica HVVDGCREFMPMPGDA cultivar-ADALKCAACGCHRSFHR group) KDDG 118 G3685 Oryza sativa HB: 172-235HB: 603-794 RKRFRTKFTPEQKEQML 1381  56% (japonica AFAERVGWRMQKQDEAcultivar- LVEQFCAQVGVRRQVFK group) VWMHNNKSSIGSSS  44 G2989 ArabidopsisZF: 50-105 ZF: 208-375 VTYKECLKNHAAAIGGH 1382  58% thalianaALDGCGEFMPSPSSTPSD PTSLKCAACGCHRNFHR RETD  44 G2989 ArabidopsisHB: 192-255 HB: 634-825 RKRFRTKFSSNQKEKMH 1383  59% thalianaEFADRIGWKIQKRDEDEV RDFCREIGVDKGVLKVW MHNNKNSFKFSG  46 G2990 ArabidopsisZF: 54-109 ZF: 206-373 FTYKECLKNHAAALGGH 1384  57% thalianaALDGCGEFMPSPSSISSDP TSLKCAACGCHRNFHRR DPD  46 G2990 ArabidopsisHB: 200-263 HB: 644-835 RKRFRTKFSQFQKEKMH 1385  57% thalianaEFAERVGWKMQKRDED DVRDFCRQIGVDKSVLK VWMHNNKNTFNRRD  66 G3001 ArabidopsisZF: 62-113 ZF: 222-377 PHYYECRKNHAADIGTT 1386  57% thalianaAYDGCGEFVSSTGEEDSL NCAACGCHRNFHREELI  66 G3001 Arabidopsis HB: 179-242HB: 573-764 VKRLKTKFTAEQIEKMR 1387  42% thaliana DYAEKLRWKVRPERQEEVEEFCVEIGVNRKNFRIW MNNHKDKIIIDE  50 G2992 Arabidopsis ZF: 29-84ZF: 85-252 VCYKECLKNHAANLGGH 1388  55% thaliana ALDGCGEFMPSPTATSTDPSSLRCAACGCHRNFHRR DPS  50 G2992 Arabidopsis HB: 156-219 HB: 466-657RKRTRTKFTPEQKIKMRA 1389  48% thaliana FAEKAGWKINGCDEKSVREFCNEVGIERGVLKVW MHNNKYSLLNGK 128 G3695 Oryza sativa ZF: 22-71ZF: 64-213 GKYKECMRNHAAAMGG 1390  51% (japonica QAFDGCGEYMPASPDSLcultivar- KCAACGCHRSFHRRAAA group) 128 G3695 Oryza sativa HB: 164-227HB: 490-681 RKRERTKFTPEQKERMRE 1391  57% (japonica FAEKQGWRINRNDDGALcultivar- DRFCVEIGVKRHVLKVW group) MHNHKNQLASSP  56 G2995 ArabidopsisZF: 3-58 ZF: 143-310 VLYNECLKNHAVSLGGH 1392  50% thalianaALDGCGEFTPKSTTILTDP PSLRCDACGCHRNFHRRS PS  56 G2995 ArabidopsisHB: 115-178 HB: 479-670 KKHKRTKFTAEQKVKMR 1393  45% thalianaGFAERAGWKINGWDEK WVREFCSEVGIERKVLK VWIHNNKYFNNGRS 124 G3692 Oryza sativaZF: 10-61 ZF: 28-183 EVYRECMRNHAAKLGTY 1394  48% (japonicaANDGCCEYTPDDGHPAG cultivar- LLCAACGCHRNFHRKDF group) L 124 G3692Oryza sativa HB: 119-188 HB: 355-564 RRRTRTKFTEEQKARML 1395  58%(japonica RFAERLGWRMPKREPGR cultivar- APGDDEVARFCREIGVNR group)QVFKVWMHNHKAGGGG GG 126 G3694 Oryza sativa ZF: 1-40 ZF: 1-120MGAHVLDGCGEFMSSPG 1396  48% (japonica DGAAALACAACGCHRSF cultivar- HRREPAgroup) 126 G3694 Oryza sativa HB: 145-208 HB: 433-624 KKRERTKFTAEQKERMR1397  56% (japonica EFAHRVGWRIHKPDAAA cultivar- VDAFCAQVGVSRRVLKV group)WMHNNKLLAKTPP  68 G3002 Arabidopsis ZF: 5-53 ZF: 81-227CVYRECMRNHAAKLGSY 1398  42% thaliana AIDGCREYSQPSTGDLCV ACGCHRSYHRRIDV 68 G3002 Arabidopsis HB: 106-168 HB: 384-572 QRRRKSKFTAEQREAMK 1399 35% thaliana DYAAKLGWTLKDKRAL REEIRVECEGIGVTRYHE KTWVNNNKKFYH %ID toG3086  16 G3086 Arabidopsis HLH/MYC: HLH/MYC: KRGCATHPRSIAERVRRT 1400100% thaliana 307-365 1059-1235 KISERMRKLQDLVPNMD TQTNTADMLDLAVQYIKDLQEQVK 188 G3767 Glycine max HLH/MYC: HLH/MYC: KRGCATHPRSIAERVRRT 1401 93% 146-204 436-612 KISERMRKLQDLVPNMD KQTNTADMLDLAVDYIK DLQKQVQ 190G3768 Glycine max HLH/MYC: HLH/MYC: KRGCATHPRSIAERVRRT 1402  93% 190-248568-744 KISERMRKLQDLVPNMD KQTNTADMLDLAVDYIK DLQKQVQ 192 G3769Glycine max HLH/MYC: HLH/MYC: KRGCATHPRSIAERVRRT 1403  93% 240-298718-894 KISERMRKLQDLVPNMD KQTNTADMLDLAVEYIK DLQNQVQ 174 G3744Oryza sativa HLH/MYC: HLH/MYC: KRGCATHPRSIAERVRRT 1404  89% (japonica71-129 211-387 RISERIRKLQELVPNMDK cultivar- QTNTADMLDLAVDYIKD group)LQKQVK 178 G3755 Zea mays HLH/MYC: HLH/MYC: KRGCATHPRSIAERVRRT 1405  89%97-155 289-465 KISERIRKLQELVPNMDK QTNTSDMLDLAVDYIKD LQKQVK  26 G592Arabidopsis HLH/MYC: HLH/MYC: KRGCATHPRSIAERVRRT 1406  88% thaliana282-340 964-1140 RISERMRKLQELVPNMD KQTNTSDMLDLAVDYIK DLQRQYK 186 G3766Glycine max HLH/MYC: HLH/MYC: KRGCATHPRSIAERVRRT 1407  88% 35-93 103-279RISERMRKLQELVPHMD KQTNTADMLDLAVEYIK DLQKQFK 172 G3742 Oryza sativaHLH/MYC: HLH/MYC: KRGCATHPRSIAERVRRT 1408  86% (japonica 199-257 595-771RISERIRKLQELVPNMEK cultivar- QTNTADMLDLAVDYIKE group) LQKQVK 198 G3782Pinus taeda HLH/MYC: HLH/MYC: KRGCATHPRSIAERVRRT 1409  80% 471-5301411-1590 RISERMRKLQELVPNSDK QTVNIADMLDEAVEYVK SLQKQVQ 176 G3746Oryza sativa HLH/MYC: HLH/MYC: KRGCATHPRSIAERERRT 1410  79% (japonica312-370 934-1110 RISKRLKKLQDLVPNMD cultivar- KQTNTSDMLDIAVTYIKE group)LQGQVE 184 G3765 Glycine max HLH/MYC: HLH/MYC: KRGFATHPRSIAERVRRT 1411 79% 147-205 439-615 RISERIRKLQELVPTMDK QTSTAEMLDLALDYIKDL QKQFK 194G3771 Glycine max HLH/MYC: HLH/MYC: KRGCATHPRSIAERVRRT 1412  79% 84-142250-426 RISDRIRKLQELVPNMDK QTNTADMLDEAVAYVKF LQKQIE  28 G1134Arabidopsis HLH/MYC: HLH/MYC: KRGCATHPRSIAERVRRT 1413  77% thaliana187-245 619-795 RISDRIRKLQELVPNMDK QTNTADMLEEAVEYVKV LQRQIQ 168 G3740Oryza sativa HLH/MYC: HLH/MYC: KRGCATHPRSIAERERRT 1414  77% (japonica141-199 421-597 RISEKLRKLQELVPNMDK cultivar- QTSTADMLDLAVEHIKG group)LQSQLQ 180 G3763 Glycine max HLH/MYC: HLH/MYC: KRGFATHPRSIAERERRT 1415 77% 161-219 481-657 RISARIKKLQDLFPKSDK QTSTADMLDLAVEYIKD LQKQVK 182G3764 Glycine max HLH/MYC: HLH/MYC: KRGFATHPRSIAERVRRT 1416  77% 370-4281108-1284 RISERIKKLQDLFPKSEKQ TSTADMLDLAVEYIKDL QQKVK 196 G3772Glycine max HLH/MYC: HLH/MYC: KRGCATHPRSIAERERRT 1417  77% 211-269631-807 RISGKLKKLQDLVPNMD KQTSYADMLDLAVQHIK GLQTQVQ  40 G2555Arabidopsis HLH/MYC: HLH/MYC: KRGCATHPRSIAERVRRT 1418  76% thaliana184-242 726-902 RISDRIRRLQELVPNMDK QTNTADMLEEAVEYVKA LQSQIQ 170 G3741Oryza sativa HLH/MYC: HLH/MYC: KRGCATHPRSIAERERRT 1419  76% (japonica288-346 862-1038 RISEKLRKLQALVPNMD cultivar- KQTSTSDMLDLAVDHIK group)GLQSQLQ  38 G2149 Arabidopsis HLH/MYC: HLH/MYC: KRGCATHPRSIAERERRT 1420 74% thaliana 286-344 927-1103 RISGKLKKLQDLVPNMD KQTSYSDMLDLAVQHIKGLQHQLQ  42 G2766 Arabidopsis HLH/MYC: HLH/MYC: KRGFATHPRSIAERERRT 1421 72% thaliana 234-292 778-954 RISGKLKKLQELVPNMD KQTSYADMLDLAVEHIKGLQHQVE

The MYB-Related Family, Including the G682 Subclade

MYB transcription factors are found in both plants and animals. TheMYB-related class of transcription factors is a heterogeneous group of54 proteins that are connected to one another through their evolutionaryrelationship with proteins containing a MYB DNA binding motif. MYBproteins share a signature DNA-binding domain of approximately 50 aminoacids that contains a series of highly conserved residues with acharacteristic spacing. Critical in the formation of the tertiarystructure of the conserved MYB motif is a series of consistently spacedtryptophan residues. Animal MYBs contain three repeats of the MYBdomain: R1, R2, and R3. Plant MYBs usually contain two imperfect MYBrepeats near their amino termini: R2 and R3 (136 in Arabidopsis genome)although there is a small subgroup of three repeat (R1R2R3) MYBs similarto those found in animals, numbering approximately five in theArabidopsis genome. Each MYB repeat has the potential to form threealpha-helical segments, resembling a helix-turn-helix structure. RepeatsR2 and R3 are responsible for the sequence-specific DNA-binding of MYBproteins (Howe et al. (1990) EMBO J. 9: 161-169). Once bound, MYBproteins function to facilitate transcriptional activation orrepression, and this sometimes involves interaction with a proteinpartner (Goff et al. (1992) Genes Dev. 6: 864-875).

G682 is a member of the MYB-related family of transcription factors.There appear to be 48 Myb-related genes in Arabidopsis. The Myb-relatedgenes are similar to the classic plant Myb(R1)R2R3 genes in that theyshare a signature DNA-binding domain sequence of approximately 45 aminoacids that contains a series of highly conserved residues with acharacteristic spacing. Unlike the Myb(R1)R2R3 genes, which generallycontain two or three Myb repeats, the majority of the Myb-related genescontain only one complete Myb domain. There are several Myb-relatedgenes that have two repeat domains, however the spacing between thedomains is greater than that seen in the Myb(R1)R2R3 family and thesequence of each domain bears a much higher similarity to the genes inthe Myb-related family than the Myb(R1)R2R3 family. The G682 codingsequence corresponds to At4G01060, annotated by the Arabidopsis Genomeinitiative. This gene is one of a five-member clade of related proteinsthat range in size from 75 to 112 amino acids. These proteins contain asingle MYB repeat. Two well characterized transcription factors,CIRCADIAN CLOCK ASSOCIATED1 (CCA1/G214) and LATE ELONGATED HYPOCOTYL(LHY/G680) are among the other MYB-related proteins that contain singleMYB repeats (Wang et al. (1997) Plant Cell. 9: 491507; Schaffer et al.(1998) Cell 93: 1219-1229).

All members of the G682 subclade were found to have epidermal cell typealterations when overexpressed in Arabidopsis; for instance, so far allcharacterized members of the clade show increased numbers of root hairscompared to wild type plants, as well as a reduction in trichome number.In addition, overexpression lines for all members of the clade showed areduction in anthocyanin accumulation in response to stress, andenhanced tolerance to abiotic stress. In the case of 35S::G682transgenic lines, an enhanced tolerance to high heat conditions wasobserved. Heat can cause osmotic stress; it is therefore consistent thatthese transgenic lines were also more tolerant to drought stress in asoil-based assay. Table 2 summarizes the data for a variety of abioticstresses with G682 and its clade members. Another common feature of allof the members of this clade that have thus far been examined(constituting a majority of the sequences appearing in the box in FIG.21) is that they enhance a plant's performance in nitrogen limitingconditions, as evidenced by altered C/N sensing and/or germinationassays in low nitrogen environments.

The difference in the phenotypic responses of the overexpression linessuggests that each of these genes could have slightly different butrelated functions in the plant. One of the G682 subclade members, G1816(TRIPTYCHON, TRY), is only partially redundant with CAPRICE (CPC;Schellmann et al. (2002) EMBO J. 21: 5036-5046). No genetic data hasbeen reported for G682, G226, or G2718 in the literature.

Epidermal cell fate specification in the root, the hypocotyl, the leafand the seed coat involves similar set of genes that presumably functionin mechanistically similar ways in the various epidermal cell types. Thesignals that specify epidermal cell fate in different parts of the plantmust therefore feed into a common signal transduction cascade. Such acascade, consisting of members of the same gene family (that haveevolved from gene duplication of common ancestors) must have adopted newand different functions to variable degrees, in different regions of theplant.

Table 2 compiles a list of genes that have been implicated in root hairand trichome cell specification through genetic and biochemicalcharacterization in Arabidopsis from the public literature as well asfrom our own discoveries.

TABLE 2 Genes implicated in root hair and trichome cell specificationGene Name CAPRICE TRY GL3 GL1 WER GL2 TTG1 (CPC) (G1816) Gene bHLH/MYCMYB- MYB- HD n/a MYB-related MYB-related Family (R1)R2R3 (R1)R2R3Loss-of- None Glabrous All cell files Ectopic hairs, All cell files Noroot hairs, wild-type Function detected are hairs glabrous are hairs,ectopic roots, ectopic glabrous trichomes trichomes Gain-of- EctopicEctopic Wild-type Wild-type Wild-type Ectopic root Ectopic root Functiontrichomes trichomes hairs, glabrous hairs, glabrous Site of Leaf LeafRoot Leaf Leaf Leaf Leaf Activity Epidermis Epidermis Epidermisepidermis, epidermis, epidermis and epidermis and root epidermis rootepidermis root epidermis root epidermis and seed coat and seed coatReference Payne et al. (Di Cristina Lee and Masucci et al., Galway etal. Wada et al. Schellmann (2000) et al. (1996) Schiefelbein (1994),(1994) (1997) et al. (2002) (1999) DiCristina et al. (1996) References:Di Cristina et al. (1996) Plant J. 10: 393-402 Galway et al (1994) Dev.Biol. 166,: 740-754 Lee and Schiefelbein (1999) Cell 99: 473-483 Masucciet al. (1994) Plant Physiol. 106: 1335-1346 Payne et al. (2000) Genetics156: 1349-1362 Schellmann et al. (2002) EMBO J. 21: 5036-5046 Wada etal. (1997) Science 277: 1113-1116

In recently proposed genetic models to explain trichome and root haircell specification, a theoretical model of lateral inhibition first putforth by Wigglesworth (1940) J. Exp. Biol. 17: 180-200) was used(Schellmann et al. (2002) supra; Lee and Schiefelbein (2002) Plant Cell14: 611-618). Lateral inhibition is a process whereby a cell that hastaken a certain fate prevents its neighbors from taking that same fate.The mechanism of lateral inhibition involves diffusible activators andrepressors. The activator complex stimulates its own expression as wellas that of the repressor. The repressor then moves across cellboundaries to suppress the activator complex found in neighboring cells.Since it is conceivable that both activator and repressor are capable ofdiffusion across cell boundaries, in this model it is proposed that therepressor is slightly smaller and therefore diffuses more quicklyresulting in the overall suppression of the activator in neighboringcells (Schellmann et al. (2002) supra). In other words, in cells wherethe proteins are initially being produced, the scales are still tippedin the direction of the activator and in the neighboring cells thescales are tipped in the direction of the repressor.

In leaf epidermal tissue, the default program is the formation of atrichome cell fate through the activity of the homeobox transcriptionfactor, GLABRA2 (GL2). GL2 is known to be induced by the proposed“activator complex” that is composed of GL1, a MYB-related protein, TTG1a WD-40 repeat containing protein, and GL3, a bHLH transcription factor.The formation of this complex is supported by genetic data as well as bybiochemical data. Yeast 2-hybrid data shows that GL3 interacts with bothTTG1 and GL1 (Payne et al. (2000) supra). A non-trichome cell fate, onthe other hand, is specified in neighboring cells through the combinedactivity of two repressors, TRY (G1816) and CPC. TRY and CPC areparalogs and most likely function in a very similar manner. However,based on the different phenotypes of try and cpc mutants with respect totrichome initiation, and the additive phenotype of the double mutant,Schellmann et al. (Schellmann et al. (2002) supra) concluded that theirfunction was slightly different, and proposed that CPC and TRY mightinteract with different proteins in the “activator complex”. This mightexplain the differences in the phenotypes observed in the mutants.

In the lateral inhibition model described above for trichome cellspecification, GL1, TTG1 and GL3 function in a regulatory feedback loop,enhancing their own expression. A complex composed of those threeproteins, activates GL2 that then functions in promoting trichome cellfate. The GL1/TTG/GL3 complex also serves to activate the repressors CPCand TRY that then results in the prevention of trichome formation inneighboring cells.

Similarly in the root epidermis, but with reverse logic, the “activatorcomplex” promotes a non-hair cell fate. In neighboring cells where therepressor activity accumulates to a greater degree, a hair cell fate isdetermined. Involvement of CPC in a lateral inhibition model in roothair cell specification was supported by a series of genetic experimentsrecently described (Lee and Schiefelbein (2002) supra). The proposed“activator” that is important for the specification of a non-root haircell fate is thought to be composed of WER (MYB-related transcriptionfactor and paralog to GL1), TTG1 and a bHLH transcription factor thathas yet to be identified. (The maize bHLH transcription factor, R, wascapable of suppressing the ttg1 root hair phenotype suggesting that asimilar bHLH is involved in this process). Genetic data supports themodel that proposes that the activator complex activates the homeodomaintranscription factor GL2 (a positive regulator of atrichoblast[non-hair] cell fate in the root). The repressor proteins in this modelare, again, postulated to be CPC and TRY (G1816). Consistent with thismodel, Lee and Schiefelbein (Lee and Schiefelbein (2002) supra) haveshown that CPC inhibits the expression of WER, GL2 and itself. They havealso shown that WER activates GL2 and CPC.

Candidate genes for the bHLH component of the “activator complex” inroot hair development are G1666 (TT8) and G581. Both genes are similarin sequence to the maize R-gene and we found that both had seedanthocyanin phenotypes when overexpressed. Anthocyanin production isconsistent with genes that potentially have maize R-like activity.

The fact that all of the G682 subclade members have slightly differentphenotypes suggests that the genes do not have completely overlapping orredundant functions in the plant. The low nitrogen and other abioticstress tolerance phenotypes in these lines may be related to theincrease in root hairs on the root epidermis. Increasing root hairdensity could provide an increase in absorptive surface area and anincrease in nitrate transporters that are normally found there.Alternatively, ectopic expression of these transcription factors mayaffect stomate formation as has been reported for wer, ttg1 and g12mutations (Hung et al. (1998) Plant Physiol. 117: 73-84; Berger et al.(1998) Dev. Biol. 194: 226-234; Lee and Schiefelbein (1999) supra). Suchalterations in stomate production could alter plant water status.Interestingly, our data also indicated that G1816 (TRY) overexpressionlines had a glucose sugar sensing phenotype. Several sugar-sensingmutants have turned out to be allelic to ABA and ethylene mutants. Thispotentially implicates G1816 in hormone signaling.

Because the G682 subclade members are short proteins that are comprisedof almost exclusively a DNA binding motif, it is possible that theyfunction as repressors. Repression could occur at the level of DNAbinding through competition with other factors at target promoters.Repression through protein-protein interactions, though, cannot beexcluded. An alternative model is that the G682 subclade membersfunction by activating a second pathway that has not yet beenidentified.

The residues in the boxes in FIG. 20B may be used to identify G682subclade members. Of the sequences examined to date, a valine(corresponding to position 50 of G682 and a glutamate residue (at aposition corresponding to position 70 of G682) were found that arepresent in members of the G682 subclade (these residues may be found inthe boxes and below the arrows in FIG. 20B) but not outside of thesubclade. All members of the clade examined thus far have thesubsequence:

E-(X)₉-L-V-G-(X)₂-W-(X)₂-I-A-G-R-(X)₂-G-R-(X)₅-E-(X)₂-W (SEQ ID NO:1422), where X is any amino acid.

Table 3 shows the G682 subclade polypeptides identified by polypeptideSEQ ID NO and Identifier (e.g., Gene ID (GID) No., accession number orother name), and includes the species from which each sequence wasderived, the coordinates of the MYB-related domains in polypeptide aminoacid coordinates and polynucleotide base coordinates, the respectivedomain sequences, and the extent of identity in percentage terms to theMYB-related domain of G682. It is of interest to note that a number ofnon-Arabidopsis monocot and dicot sequences are more similar to 6682than a number of the Arabidopsis paralogs that are functionally similarto G682.

TABLE 3Gene families and binding domains for exemplary sequences altering C/N sensing,including paralogs and orthologs Polypeptide Polypeptide SEQ ID % ID toAmino Acid Base NO: of MYB- Coordinates Coordinates Myb- related SEQof the MYB- of the MYB- related Domain ID Iden- related relatedMYB-related Domain of NO: tifier Species Domain Domain Domain SequenceSequence G682 234 G682 Arabidopsis 33-77  99-233 VNMSQEEEDLVSRMH 1423100% thaliana KLVGDRWELIAGRIPG RTAGEIERFWVMKN 324 G2718 Arabidopsis32-76  94-228 IAMAQEEEDLICRMYK 1424  80% thaliana LVGERWDLIAGRIPGRTAEEIERFWVMKN 328 G3393 Oryza sativa 31-75 172-306 VHFTEEEEDLVFRMHR 1425 71% (japonica LVGNRWELIAGRIPGRT cultivar- AKEVEMFWAVKH group) 326 G3392Oryza sativa 32-76 143-277 VHFTEEEEDIVFRMHRL 1426  68% (japonicaVGNRWELIAGRIPGRT cultivar- AEEVEKFWAIKH group) 360 G3431 Zea mays 31-75 94-228 VDFTEAEEDLVSRMHR 1427  68% LVGNRWEIIAGRIPGRT AEEVEMFWSKKY 370G3444 Zea mays 31-75 104-238 VDFTEAEEDLVSRMHR 1428  68%LVGNRWEIIAGRIPGRT AEEVEMFWSKKY 382 G3450 Glycine max 20-64  83-217IHMSEQEEDLIRRMYK 1429  68% LVGDKWNLIAGRIPGR KAEEIERFWIMRH 312 G1816Arabidopsis 30-74  88-222 INMIEQEEDLIFRMYRL 1430  64% thalianaVGDRWDLIAGRVPGRQ PEEIERYWIMRN 286 G226 Arabidopsis 38-82 121-255ISMTEQEEDLISRMYRL 1431  62% thaliana VGNRWDLIAGRVVGR KANEIERYWIMRN 380G3449 Glycine max 26-70  95-229 VEFSEDEETLIIRMYKL 1432  62%VGERWSLIAGRIPGRTA EEIEKYWTSRF 378 G3448 Glycine max 26-70  96-230VEFSEDEETLIIRMYKL 1433  60% VGERWSIIAGRIPGRTA EEIEKYWTSRF 372 G3445Glycine max 25-69  89-223 VEFSEAEEILIAMVYNL 1434  55% VGERWSLIAGRIPGRTAEEIEKYWTSRF 374 G3446 Glycine max 26-70  92-226 VEFSEAEEILIAMVYNL 1435 55% VGERWSLIAGRIPGRTA EEIEKYWTSRF 376 G3447 Glycine max 26-70  85-219VEFSEAEEILIAMVYNL 1436  55% VGERWSLIAGRIPGRTA EEIEKYWTSRF

Table 4 shows polypeptides of the invention identified by SEQ ID NO;Identifier (for example, Gene ID (GID) No); the transcription factorfamily to which the polypeptide belongs, and conserved domains of thepolypeptide. The first column shows the polypeptide SEQ ID NO; the thirdcolumn shows the transcription factor family to which the polynucleotidebelongs; and the fourth column shows the amino acid residue positions ofthe conserved domain in amino acid (AA) coordinates.

TABLE 4 Gene families and conserved domains Poly- peptide ConservedDomains SEQ ID in Amino NO: Identifier Family Acid Coordinates 224 G175WRKY 178-234, 372-428 226 G303 HLH/MYC 92-161 228 G354 Z-C2H2 42-62,88-109 230 G489 CAAT 57-156 232 G634 TH 62-147, 189-245 234 G682MYB-related 27-63  236 G916 WRKY 293-349  238 G975 AP2 4-71 240 G1069AT-hook 67-75, 76-218 242 G1452 NAC 55-196 244 G1820 CAAT 70-133 246G2701 MYB-related 33-81, 129-183 248 G2789 AT-hook 59-67, 68-208 250G2839 Z-C2H2 34-60, 85-113 252 G2854 ACBF-like 110-250  254 G3083bZIP-ZW2 75-105, 188-215 256 G184 WRKY 295-352  258 G186 WRKY 312-369 260 G353 Z-C2H2 41-61, 84-104 262 G512 NAC 24-166 264 G596 AT-hook 89-96266 G714 CAAT 58-148 268 G877 WRKY 272-328, 487-603 270 G1357 NAC 17-158272 G1387 AP2 4-71 274 G1634 MYB-related 129-180  276 G1889 Z-C2H280-100 278 G1940 ACBF-like 156-228  280 G1974 Z-C2H2 32-60, 72-116 282G2153 AT-hook 75-94, 162-206 284 G2583 AP2 4-71 286 G226 MYB-related28-78  288 G481 CAAT 20-109 290 G482 CAAT 25-116 292 G485 CAAT 21-116294 G486 CAAT 5-66 296 G1067 AT-hook 86-92, 94-247 298 G1070 AT-hook98-120 300 G1073 AT-hook 34-42, 43-187 302 G1075 AT-hook 78-85  304G1076 AT-hook 82-89  306 G1248 CAAT 46-155 308 G1364 CAAT 29-118 310G1781 CAAT 35-130 312 G1816 MYB-related 31-81  314 G1945 AT-hook 49-71 316 G2155 AT-hook 18-38  318 G2156 AT-hook 72-78, 80-232 320 G2345 CAAT26-152 322 G2657 AT-hook 116-129  324 G2718 MYB-related 21-76  326 G3392MYB-related 21-72  328 G3393 MYB-related 20-71  330 G3394 CAAT 37-126332 G3395 CAAT 19-108 334 G3396 CAAT 21-110 338 G3397 CAAT 23-112 338G3398 CAAT 21-110 340 G3399 AT-hook 99-107, 108-253 342 G3400 AT-hook83-89, 91-237 344 G3401 AT-hook 35-41, 43-186 346 G3403 AT-hook 58-64,66-207 348 G3404 AT-hook 111-117,119-263 350 G3405 AT-hook 97-103,105-248 352 G3406 AT-hook 82-88, 90-232 354 G3407 AT-hook 63-71, 72-220356 G3408 AT-hook 83-89, 91-247 358 G3429 CAAT 35-124 360 G3431MYB-related 20-71  362 G3434 CAAT 18-107 364 G3435 CAAT 22-111 366 G3436CAAT 20-109 368 G3437 CAAT 54-143 370 G3444 MYB-related 20-71  372 G3445MYB-related 15-65  374 G3446 MYB-related 16-66  376 G3447 MYB-related16-66  378 G3448 MYB-related 15-66  380 G3449 MYB-related 15-66  382G3450 MYB-related 9-60 384 G3456 AT-hook 44-52, 53-195 386 G3458 AT-hook56-62, 64-207 388 G3459 AT-hook 77-85, 86-228 390 G3460 AT-hook 74-82,83-225 392 G3462 AT-hook 82-88, 90-237 394 G3470 CAAT 27-116 396 G3471CAAT 26-115 398 G3472 CAAT 25-114 400 G3473 CAAT 23-113 402 G3474 CAAT25-114 404 G3475 CAAT 23-112 406 G3476 CAAT 26-115 408 G3477 CAAT 27-116410 G3478 CAAT 23-112 412 G3556 AT-hook 45-51, 53-196 414 G3835 CAAT4-92 416 G3836 CAAT 34-122 418 G3837 CAAT 35-123 420 G24 AP2 25-92  422G154 MADS 2-57 424 G384 HB 14-77  294 G486 CAAT 5-66 426 G545 Z-C2H282-102, 136-154 428 G760 NAC 12-156 430 G773 NAC 17-159 432 G937 GARP197-246  434 G971 AP2 120-186  436 G988 SCR 146-217, 278-366, 370-444438 G989 SCR 121-186, 238-327, 326-399 240 G1069 AT-hook 67-74  440G1090 AP2 17-84  442 G1322 MYB-(R1)R2R3 26-30  444 G1587 HB 61-121 446G1666 HLH/MYC 353-420  448 G1700 RING/C3H2C3 93-134 450 G1818 CAAT36-113 452 G1868 GRF-like 164-270  454 G1888 Z-CO-like 5-50 456 G2117bZIP 46-106 458 G2131 AP2 50-121, 146-217 460 G2520 HLH/MYC 135-206  462G2522 AT-hook At-hooks: 101-109 & 134-142 2nd domain: 143-291 248 G2789AT-hook 53-73, 121-165 464 G8 AP2 151-217,243-293 466 G27 AP2 37-104 468G156 MADS 2-57 470 G161 MADS 6-62 472 G168 MADS 1-57 474 G183 WRKY307-368  476 G189 WRKY 240-297  478 G200 MYB-(R1)R2R3 12-116 480 G234MYB-(R1)R2R3 14-115 482 G237 MYB-(R1)R2R3 11-113 484 G275 AKR 308-813 486 G326 Z-CO-like 11-94, 354-400 488 G347 Z-LSDlike 9-39, 50-70, 80-127490 G427 HB 307-370  492 G505 NAC 20-170 494 G590 HLH/MYC 202-254  496G602 DBP 110-162  498 G618 TEO 32-89  500 G635 TH 239-323  502 G643 TH47-85  504 G653 Z-LIM 10-61, 109-160 506 G657 MYB-(R1)R2R3 35-187 508G837 AKR 250-754  510 G866 WRKY 43-300 512 G872 AP2 18-84  514 G904RING/C3H2C3 117-158  516 G912 AP2 51-118 518 G932 MYB-(R1)R2R3 14-118520 G958 NAC  7-156 522 G964 HB 126-186  238 G975 AP2 4-71 524 G979 AP263-139, 165-233 526 G1049 bZIP 77-132 528 G1246 MYB-(R1)R2R3 27-139 530G1255 Z-CO-like 18-56  532 G1266 AP2 79-147 534 G1331 MYB-(R1)R2R3 8-109 536 G1332 MYB-(R1)R2R3 13-116 538 G1494 HLH/MYC 261-311  540G1535 HB 109-169  542 G1649 HLH/MYC 225-295  544 G1750 AP2 115-182  546G1773 RING/C3HC4 139-184  548 G1835 GATA/Zn 224-296  550 G1930 AP259-124, 179-273 10 G2053 NAC  6-152 552 G2057 TEO 46-103 12 G2133 AP210-77  554 G2144 HLH/MYC 203-283  556 G2145 HLH/MYC 166-243  558 G2295MADS 1-57 560 G2512 AP2 79-147 562 G2531 NAC 52-212 564 G2535 NAC 11-114566 G2590 MADS 2-57 568 G2719 MYB-(R1)R2R3 56-154 570 G9 AP2 62-127,184-277 572 G12 AP2 27-94  574 G40 AP2 45-112 576 G41 AP2 39-106 578 G42AP2 48-115 2 G47 AP2 10-75  580 G170 MADS 2-57 582 G216 MYB-(R1)R2R349-151 584 G221 MYB-(R1)R2R3 21-125 586 G232 MYB-(R1)R2R3 14-115 588G249 MYB-(R1)R2R3 19-116 590 G256 MYB-(R1)R2R3 13-115 592 G350 Z-C2H291-113, 150-170 594 G351 Z-C2H2 77-97, 118-140 596 G385 HB 60-123 598G389 HB 84-147 600 G398 HB 128-191  602 G399 HB 126-186  604 G425 HB305-365  606 G426 HB 346-406  608 G440 AP2 122-189  610 G441 AP2 40-10720 G515 NAC  6-149 22 G516 NAC  6-141 24 G517 NAC  6-153 612 G518 NAC 7-153 614 G572 bZIP 120-186  264 G596 AT-hook 89-96  616 G654 Z-LIM10-61, 108-159 618 G666 MYB-(R1)R2R3 14-118 620 G668 MYB-(R1)R2R3 13-113622 G759 NAC 17-159 624 G789 HLH/MYC 253-313  626 G829 AKR 250-754  628G864 AP2 119-186  630 G867 AP2 59-124, 184-276 632 G883 WRKY 245-302 634 G914 AP2 106-162, 198-238 636 G957 NAC 12-182 638 G961 NAC 12-180640 G993 AP2 69-134, 191-290 642 G1011 MADS 2-57 644 G1065 DBP 101-210 646 G1071 AT-hook 98-111, 132-138, 140-286 648 G1277 AP2 18-85  650G1309 MYB-(R1)R2R3  9-114 652 G1337 Z-CO-like 9-75 654 G1379 AP2 18-85 656 G1386 AP2 42-109 272 G1387 AP2 4-71 658 G1412 NAC 13-162 660 G1439GRF-like 133-239  662 G1482 Z-CO-like 5-63 664 G1484 Z-CO-like 16-39 666 G1588 HB 66-124 668 G1752 AP2 83-151 670 G1836 CAAT 30-164 672 G1942HLH/MYC 178-270  674 G2065 MADS 1-57 676 G2106 AP2 56-139, 165-233 678G2107 AP2 27-94  680 G2148 HLH/MYC 130-268  282 G2153 AT-hook 75-94,162-206 682 G2180 NAC  7-156 684 G2513 AP2 27-94  686 G2545 HB 215-278 688 G2576 AP2 9-75 284 G2583 AP2 4-71 690 G3041 NAC  8-136 692 G3362 AP241-108 694 G3364 AP2 51-114 696 G3365 AP2 41-108 698 G3366 AP2 53-117700 G3367 AP2 51-114 702 G3368 AP2 51-120 704 G3369 AP2 107-170  706G3370 AP2 29-99  708 G3371 AP2 36-102 710 G3372 AP2 30-95  712 G3373 AP243-109 714 G3374 AP2 51-118 716 G3375 AP2 49-113 718 G3376 AP2 51-115720 G3377 AP2 41-107 722 G3378 AP2 83-154 724 G3379 AP2 47-119 726 G3384MYB-(R1)R2R3 14-118 728 G3385 MYB-(R1)R2R3 14-118 730 G3386 MYB-(R1)R2R314-118 732 G3388 AP2 66-129, 181-274 734 G3389 AP2 64-129, 177-266 736G3390 AP2 66-131, 192-294 738 G3391 AP2 79-148,215-300 344 G3401 AT-hook35-41, 43-186 346 G3403 AT-hook 58-64, 66-207 740 G3432 AP2 75-140,212-299 742 G3433 AP2 80-151,210-291 744 G3438 AP2 50-116 746 G3439 AP257-126 748 G3440 AP2 49-116 750 G3441 AP2 55-120 752 G3442 AP2 61-127754 G3451 AP2 80-141, 209-308 756 G3452 AP2 51-116, 171-266 758 G3453AP2 57-122, 177-272 760 G3454 AP2 74-141, 203-302 384 G3456 AT-hook44-50, 52-195 392 G3462 AT-hook 82-88, 90-237 762 G3463 AP2 60-125 764G3464 AP2 50-114 766 G3465 AP2 61-125 768 G3466 AP2 63-127 770 G3467 AP260-123 772 G3468 AP2 63-128 774 G3469 AP2 16-79  776 G3497 AP2 51-114778 G3498 AP2 50-114 780 G3499 AP2 46-111 782 G3500 MYB-(R1)R2R3 14-118784 G3501 MYB-(R1)R2R3 14-118 786 G3502 MYB-(R1)R2R3 14-119 788 G3537MYB-(R1)R2R3 14-118 790 G3538 MYB-(R1)R2R3 13-117 792 G3539 MYB-(R1)R2R314-118 794 G3540 MYB-(R1)R2R3 14-118 796 G3541 MYB-(R1)R2R3 14-118 412G3556 AT-hook 45-51, 53-196 88 G3643 AP2 13-78  90 G3644 AP2 52-122 92G3645 AP2 10-75  94 G3646 AP2 10-77  96 G3647 AP2 13-78  98 G3649 AP215-87  100 G3651 AP2 60-130 798 G3652 AP2 13-78  800 G3653 AP2 41-107802 G3654 AP2 9-76 804 G3655 AP2 31-96  806 G3656 AP2 23-86  232 G634 TH62-147, 189-245, 808 G1048 bZIP 138-190  810 G1100 RING/C3H2C3 96-137658 G1412 NAC 13-162 812 G1796 AP2 54-121 814 G1995 Z-C2H2 93-113 816G2467 HS 28-119 818 G2505 NAC  9-137 820 G2550 HB 345-408  822 G2640 SRS146-189  824 G2686 WRKY 122-173  248 G2789 AT-hook 53-73, 121-165, 420G24 AP2 25-92  826 G38 AP2 76-143 828 G44 AP2 85-154 830 G230MYB-(R1)R2R3 13-114 480 G234 MYB-(R1)R2R3 14-115 832 G261 HS 15-106 834G271 AKR 41-106, 325-363, 226 G303 HLH/MYC 92-161 836 G359 Z-C2H2 49-69 838 G377 RING/C3H2C3 85-128 840 G388 HB 98-158 842 G435 HB 4-67 844 G442AP2 66-138 846 G468 IAA 86-102, 141-171, 848 G571 bZIP 160-220, 441-452,850 G652 Z-CLDSH 28-49, 137-151, 182-196, 852 G664 MYB-(R1)R2R3 14-116854 G772 NAC 27-176 856 G798 Z-Dof 19-47  858 G818 HS 71-162 434 G971AP2 120-186  860 G974 AP2 80-147 436 G988 SCR 146-217, 278-366, 370-444,862 G1062 HLH/MYC 308-359  240 G1069 AT-hook 67-74  864 G1129 HLH/MYC171-244  866 G1137 HLH/MYC 264-314  868 G1425 NAC 20-173 870 G1517RING/C3HC4 312-349  872 G1655 HLH/MYC 134-192  874 G1743 RING/C3H2C394-136 876 G1789 MYB-related 12-62  878 G1806 bZIP 165-225  880 G1911MYB-related 12-62  882 G2011 HS 55-146 316 G2155 AT-hook 18-38  884G2215 bZIP-NIN 150-246  886 G2452 MYB-related 28-79, 146-194, 888 G2455YABBY 10-48, 107-154, 890 G2510 AP2 42-109 892 G2515 MADS 1-57 894 G2571AP2 133-200  896 G2702 MYB-(R1)R2R3 31-131 898 G2763 HLH/MYC 140-210 900 G2774 HLH/MYC 157-227  892 G2888 Z-C2H2 41-61, 120-140, 904 G2958IAA 88-104, 143-172, 906 G5 AP2 149-216  572 G12 AP2 27-94  908 G197MYB-(R1)R2R3 14-116 910 G207 MYB-(R1)R2R3  6-106 912 G227 MYB-(R1)R2R313-112 586 G232 MYB-(R1)R2R3 14-115 914 G242 MYB-(R1)R2R3  6-105 916G255 MYB-(R1)R2R3 14-116 918 G265 HS 13-104 920 G361 Z-C2H2 43-63  922G362 Z-C2H2 62-82  924 G370 Z-C2H2 97-117 926 G504 NAC 16-178 928 G554bZIP 82-142 930 G555 bZIP 38-110 932 G556 bZIP 83-143 934 G558 bZIP45-105 936 G578 bZIP 36-96  264 G596 AT-hook 89-96  938 G629 bZIP 92-152622 G759 NAC 17-159 430 G773 NAC 17-159 940 G776 NAC 27-175 942 G812 HS29-120 634 G914 AP2 106-162, 198-238, 944 G997 MYB-related 9-59 946G1133 HLH/MYC 256-326  948 G1141 AP2 75-142 950 G1198 bZIP 173-223  648G1277 AP2 18-85  952 G1335 Z-CLDSH 24-43, 131-144, 185-203, 654 G1379AP2 18-85  954 G1454 NAC  9-178 956 G1664 HLH/MYC 258-328  958 G1897Z-Dof 34-62  314 G1945 AT-hook 49-71  960 G1991 Z-C2H2 6-26, 175-195,224-226, 282 G2153 AT-hook 75-94, 162-206, 962 G2216 bZIP-NIN 90-139 964G2546 HB 349-413  966 G2586 WRKY 103-160  968 G2587 WRKY 108-165  970G2635 NAC  8-161 972 G2639 SRS 114-167  974 G2642 SRS 54-97  976 G2721MYB-related 10-60  978 G2826 Z-C2H2 75-95  980 G2838 Z-C2H2 57-77  982G2866 IAA 84-100, 139-168, 344 G3401 AT-hook 35-41, 43-186, 346 G3403AT-hook 58-64, 66-207, 348 G3408 AT-hook 83-89, 91-247, 384 G3456AT-hook 44-50, 52-195, 392 G3462 AT-hook 82-88, 90-237, 984 G3503MYB-(R1)R2R3 14-116 986 G3504 MYB-(R1)R2R3 14-116 988 G3505 MYB-(R1)R2R314-116 990 G3506 MYB-(R1)R2R3 14-116 992 G3507 MYB-(R1)R2R3 14-116 994G3508 MYB-(R1)R2R3 14-116 996 G3509 MYB-(R1)R2R3 14-116 998 G3527MYB-(R1)R2R3 13-117 1000 G3528 MYB-(R1)R2R3 13-117 1002 G3529MYB-(R1)R2R3 14-116 1004 G3531 MYB-(R1)R2R3 14-116 1006 G3532MYB-(R1)R2R3 14-116 1008 G3533 MYB-(R1)R2R3 14-116 1010 G3534MYB-(R1)R2R3 14-116 412 G3556 AT-hook 45-51, 53-196, 806 G3656 AP223-86  1012 G3809 NAC 25-236

Producing Polypeptides

The polynucleotides of the invention include sequences that encodetranscription factors and transcription factor homolog polypeptides andsequences complementary thereto, as well as unique fragments of codingsequence, or sequence complementary thereto. Such polynucleotides canbe, for example, DNA or RNA, the latter including mRNA, cRNA, syntheticRNA, genomic DNA, cDNA synthetic DNA, oligonucleotides, etc. Thepolynucleotides are either double-stranded or single-stranded, andinclude either, or both sense (i.e., coding) sequences and antisense(i.e., non-coding, complementary) sequences. The polynucleotides includethe coding sequence of a transcription factor, or transcription factorhomolog polypeptide, in isolation, in combination with additional codingsequences (for example, a purification tag, a localization signal, as afusion-protein, as a pre-protein, or the like), in combination withnon-coding sequences (for example, introns or inteins, regulatoryelements such as promoters, enhancers, terminators, and the like),and/or in a vector or host environment in which the polynucleotideencoding a transcription factor or transcription factor homologpolypeptide is an endogenous or exogenous gene.

A variety of methods exist for producing the polynucleotides of theinvention. Procedures for identifying and isolating DNA clones are wellknown to those of skill in the art, and are described in, for example,Berger and Kimmel, Guide to Molecular Cloning Techniques, Methods inEnzymology, vol. 152 Academic Press, Inc., San Diego, Calif. (“Berger”);Sambrook et al. Molecular Cloning—A Laboratory Manual (2nd ed.), Vol.1-3, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y., 1989(“Sambrook”) and Current Protocols in Molecular Biology, Ausubel et al.eds., Current Protocols, a joint venture between Greene PublishingAssociates, Inc. and John Wiley & Sons, Inc., (supplemented through2000) (“Ausubel”).

Alternatively, polynucleotides of the invention, can be produced by avariety of in vitro amplification methods adapted to the presentinvention by appropriate selection of specific or degenerate primers.Examples of protocols sufficient to direct persons of skill through invitro amplification methods, including the polymerase chain reaction(PCR) the ligase chain reaction (LCR), Qβ-replicase amplification andother RNA polymerase mediated techniques (for example, NASBA), forexample, for the production of the homologous nucleic acids of theinvention are found in Berger (supra), Sambrook (supra), and Ausubel(supra), as well as Mullis et al. (1987) PCR Protocols A Guide toMethods and Applications (Innis et al. eds) Academic Press Inc. SanDiego, Calif. (1990) (Innis). Improved methods for cloning in vitroamplified nucleic acids are described in Wallace et al. U.S. Pat. No.5,426,039. Improved methods for amplifying large nucleic acids by PCRare summarized in Cheng et al. (1994) Nature 369: 684-685 and thereferences cited therein, in which PCR amplicons of up to 40 kb aregenerated. One of skill will appreciate that essentially any RNA can beconverted into a double-stranded DNA suitable for restriction digestion,PCR expansion and sequencing using reverse transcriptase and apolymerase (for example, in Ausubel, Sambrook and Berger, all supra).

Alternatively, polynucleotides and oligonucleotides of the invention canbe assembled from fragments produced by solid-phase synthesis methods.Typically, fragments of up to approximately 100 bases are individuallysynthesized and then enzymatically or chemically ligated to produce adesired sequence, for example, a polynucleotide encoding all or part ofa transcription factor. For example, chemical synthesis using thephosphoramidite method is described, for example, by Beaucage et al.(1981) Tetrahedron Letters 22: 1859-1869; and Matthes et al. (1984) EMBOJ. 3: 801-805. According to such methods, oligonucleotides aresynthesized, purified, annealed to their complementary strand, ligatedand then optionally cloned into suitable vectors. And if so desired, thepolynucleotides and polypeptides of the invention can be custom orderedfrom any of a number of commercial suppliers.

Homologous Sequences

Sequences homologous, i.e., that share significant sequence identity orsimilarity, to those provided in the Sequence Listing, derived fromArabidopsis thaliana or from other plants of choice, are also an aspectof the invention. Homologous sequences can be derived from any plantincluding monocots and dicots and in particular agriculturally importantplant species, including but not limited to, crops such as soybean,wheat, corn (maize), potato, cotton, rice, rape, oilseed rape (includingcanola), sunflower, alfalfa, clover, sugarcane, and turf; or fruits andvegetables, such as banana, blackberry, blueberry, strawberry, andraspberry, cantaloupe, carrot, cauliflower, coffee, cucumber, eggplant,grapes, honeydew, lettuce, mango, melon, onion, papaya, peas, peppers,pineapple, pumpkin, spinach, squash, sweet corn, tobacco, tomato,tomatillo, watermelon, rosaceous fruits (such as apple, peach, pear,cherry and plum) and vegetable brassicas (such as broccoli, cabbage,cauliflower, Brussels sprouts, and kohlrabi). Other crops, includingfruits and vegetables, whose phenotype can be changed and which comprisehomologous sequences include barley; rye; millet; sorghum; currant;avocado; citrus fruits such as oranges, lemons, grapefruit andtangerines, artichoke, cherries; nuts such as the walnut and peanut;endive; leek; roots such as arrowroot, beet, cassava, turnip, radish,yam, and sweet potato; and beans. The homologous sequences may also bederived from woody species, such as pine, poplar and eucalyptus, or mintor other labiates. In addition, homologous sequences may be derived fromplants that are evolutionarily related to crop plants, but which may nothave yet been used as crop plants. Examples include deadly nightshade(Atropa belladona), related to tomato; jimson weed (Datura strommium),related to peyote; and teosinte (Zea species), related to corn (maize).

Orthologs and Paralogs

Homologous sequences as described above can comprise orthologous orparalogous sequences. Several different methods are known by those ofskill in the art for identifying and defining these functionallyhomologous sequences. Three general methods for defining orthologs andparalogs are described; an ortholog, paralog or homolog may beidentified by one or more of the methods described below.

Within a single plant species, gene duplication may cause two copies ofa particular gene, giving rise to two or more genes with similarsequence and often similar function known as paralogs. A paralog istherefore a similar gene formed by duplication within the same species.Paralogs typically cluster together or in the same Glade (a group ofsimilar genes) when a gene family phylogeny is analyzed using programssuch as CLUSTAL (Thompson et al. (1994) Nucleic Acids Res. 22:4673-4680; Higgins et al. (1996) Methods Enzymol. 266: 383-402). Groupsof similar genes can also be identified with pair-wise BLAST analysis(Feng and Doolittle (1987) J. Mol. Evol. 25: 351-360). For example, aclade of very similar MADS domain transcription factors from Arabidopsisall share a common function in flowering time (Ratcliffe et al. (2001)Plant Physiol. 126: 122-132), and a group of very similar AP2 domaintranscription factors from Arabidopsis are involved in tolerance ofplants to freezing (Gilmour et al. (1998) Plant J. 16: 433-442).Analysis of groups of similar genes with similar function that fallwithin one clade can yield sub-sequences that are particular to theclade. These sub-sequences, known as consensus sequences, can not onlybe used to define the sequences within each clade, but define thefunctions of these genes; genes within a clade may contain paralogoussequences, or orthologous sequences that share the same function (forexample, in Mount (2001), in Bioinformatics: Sequence and GenomeAnalysis Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.,page 543).

Speciation, the production of new species from a parental species, canalso give rise to two or more genes with similar sequence and similarfunction. These genes, termed orthologs, often have an identicalfunction within their host plants and are often interchangeable betweenspecies without losing function. Because plants have common ancestors,many genes in any plant species will have a corresponding orthologousgene in another plant species. Once a phylogenic tree for a gene familyof one species has been constructed using a program such as CLUSTAL(Thompson et al. (1994) Nucleic Acids Res. 22: 4673-4680; Higgins et al.(1996) supra) potential orthologous sequences can be placed into thephylogenetic tree and their relationship to genes from the species ofinterest can be determined. Orthologous sequences can also be identifiedby a reciprocal BLAST strategy. Once an orthologous sequence has beenidentified, the function of the ortholog can be deduced from theidentified function of the reference sequence.

Transcription factor gene sequences are conserved across diverseeukaryotic species lines (Goodrich et al. (1993) Cell 75: 519-530; Linet al. (1991) Nature 353: 569-571; Sadowski et al. (1988) Nature 335:563-564). Plants are no exception to this observation; diverse plantspecies possess transcription factors that have similar sequences andfunctions.

Orthologous genes from different organisms have highly conservedfunctions, and very often essentially identical functions (Lee et al.(2002) Genome Res. 12: 493-502; Remm et al. (2001) J. Mol. Biol. 314:1041-1052). Paralogous genes, which have diverged through geneduplication, may retain similar functions of the encoded proteins. Insuch cases, paralogs can be used interchangeably with respect to certainembodiments of the instant invention (for example, transgenic expressionof a coding sequence). An example of such highly related paralogs is theCBF family, with four well-defined members in Arabidopsis (CBF 1, CBF2,CBF3 and CBF4) and at least one ortholog in Brassica napus, all of whichcontrol pathways involved in both freezing and drought stress (Gilmouret al. (1998) Plant J. 16: 433-442; Jaglo et al. (1998) Plant Physiol.127: 910-917).

The following references represent a small sampling of the many studiesthat demonstrate that conserved transcription factor genes from diversespecies are likely to function similarly (i.e., regulate similar targetsequences and control the same traits), and that transcription factorsmay be transformed into diverse species to confer or improve traits.

-   -   (1) Distinct Arabidopsis transcription factors, including G28        (U.S. Pat. No. 6,664,446), G482 (US Patent Application        20040045049; SEQ ID NO: 290 in the present Sequence Listing),        G867 (US Patent Application 20040098764; SEQ ID NO: 630 in the        present Sequence Listing), and G1073 (US Patent Application        20040128712; SEQ ID NO: 300 in the present Sequence Listing),        have been shown to confer abiotic stress tolerance when the        sequences are overexpressed. The polypeptides sequences belong        to distinct clades of transcription factor polypeptides that        include members from diverse species. In each case, a        significant number of sequences derived from both dicots and        monocots have been shown to confer tolerance to various abiotic        stresses when the sequences were overexpressed.    -   (2) The Arabidopsis NPR1 gene regulates systemic acquired        resistance (SAR) (Cao et al. (1997) Cell 88: 57-63);        over-expression of NPR1 leads to enhanced resistance in        Arabidopsis. When either Arabidopsis NPR1 or the rice NPR1        ortholog was overexpressed in rice (which, as a monocot, is        diverse from Arabidopsis), challenge with the rice bacterial        blight pathogen Xanthomonas oryzae pv. Oryzae, the transgenic        plants displayed enhanced resistance (Chern et al. (2001)        Plant J. 27: 101-113). NPR1 acts through activation of        expression of transcription factor genes, such as TGA2 (Fan and        Dong (2002) Plant Cell 14: 1377-1389).

(3) E2F genes are involved in transcription of plant genes forproliferating cell nuclear antigen (PCNA). Plant E2Fs share a highdegree of similarity in amino acid sequence between monocots and dicots,and are even similar to the conserved domains of the animal E2Fs. Suchconservation indicates a functional similarity between plant and animalE2Fs. E2F transcription factors that regulate meristem development actthrough common cis-elements, and regulate related (PCNA) genes (Kosugiand Ohashi, (2002) Plant J. 29: 45-59).

-   -   (4) The ABI5 gene (ABA insensitive 5) encodes a basic leucine        zipper factor required for ABA response in the seed and        vegetative tissues. Co-transformation experiments with ABI5 cDNA        constructs in rice protoplasts resulted in specific        transactivation of the ABA-inducible wheat, Arabidopsis, bean,        and barley promoters. These results demonstrate that        sequentially similar ABI5 transcription factors are key targets        of a conserved ABA signaling pathway in diverse plants. (Gampala        et al. (2001) J. Biol. Chem. 277: 1689-1694).    -   (5) Sequences of three Arabidopsis GAMYB-like genes were        obtained on the basis of sequence similarity to GAMYB genes from        barley, rice, and L. temulentum. These three Arabidopsis genes        were determined to encode transcription factors (AtMYB33,        AtMYB65, and AtMYB101) and could substitute for a barley GAMYB        and control α-amylase expression (Gocal et al. (2001) Plant        Physiol. 127: 1682-1693).    -   (6) The floral control gene LEAFY from Arabidopsis can        dramatically accelerate flowering in numerous dictoyledonous        plants. Constitutive expression of Arabidopsis LEAFY also caused        early flowering in transgenic rice (a monocot), with a heading        date that was 26-34 days earlier than that of wild-type plants.        These observations indicate that floral regulatory genes from        Arabidopsis are useful tools for heading date improvement in        cereal crops (He et al. (2000) Transgenic Res. 9: 223-227).    -   (7) Bioactive gibberellins (GAs) are essential endogenous        regulators of plant growth. GA signaling tends to be conserved        across the plant kingdom. GA signaling is mediated via GAI, a        nuclear member of the GRAS family of plant transcription        factors. Arabidopsis GAI has been shown to function in rice to        inhibit gibberellin response pathways (Fu et al. (2001) Plant        Cell 13: 1791-1802).    -   (8) The Arabidopsis gene SUPERMAN (SUP), encodes a putative        transcription factor that maintains the boundary between stamens        and carpels. By over-expressing Arabidopsis SUP in rice, the        effect of the gene's presence on whorl boundaries was shown to        be conserved. This demonstrated that SUP is a conserved        regulator of floral whorl boundaries and affects cell        proliferation (Nandi et al. (2000) Curr. Biol. 10: 215-218).    -   (9) Maize, petunia and Arabidopsis myb transcription factors        that regulate flavonoid biosynthesis are genetically similar and        affect the same trait in their native species; therefore,        sequence and function of these myb transcription factors        correlate with each other in these diverse species (Borevitz et        al. (2000) Plant Cell 12: 2383-2394).    -   (10) Wheat reduced height-1 (Rht-B1/Rht-D1) and maize dwarf-8        (d8) genes are orthologs of the Arabidopsis gibberellin        insensitive (GAI) gene. Both of these genes have been used to        produce dwarf grain varieties that have improved grain yield.        These genes encode proteins that resemble nuclear transcription        factors and contain an SH2-like domain, indicating that        phosphotyrosine may participate in gibberellin signaling.        Transgenic rice plants containing a mutant GAI allele from        Arabidopsis have been shown to produce reduced responses to        gibberellin and are dwarfed, indicating that mutant GAI        orthologs could be used to increase yield in a wide range of        crop species (Peng et al. (1999) Nature 400: 256-261).

Transcription factors that are homologous to the listed sequences willtypically share at least about 70% amino acid sequence identity in theirconserved domain. More closely related transcription factors can shareat least about 79% or about 90% or about 95% or about 98% or moresequence identity with the listed sequences, or with the listedsequences but excluding or outside a known consensus sequence orconsensus DNA-binding site, or with the listed sequences excluding oneor all conserved domains. Factors that are most closely related to thelisted sequences share, for example, at least about 85%, about 90% orabout 95% or more % sequence identity to the listed sequences, or to thelisted sequences but excluding or outside a known consensus sequence orconsensus DNA-binding site or outside one or all conserved domain. Atthe nucleotide level, the sequences will typically share at least about40% nucleotide sequence identity, preferably at least about 50%, about60%, about 70% or about 80% sequence identity, and more preferably about85%, about 90%, about 95% or about 97% or more sequence identity to oneor more of the listed sequences, or to a listed sequence but excludingor outside a known consensus sequence or consensus DNA-binding site, oroutside one or all conserved domain. The degeneracy of the genetic codeenables major variations in the nucleotide sequence of a polynucleotidewhile maintaining the amino acid sequence of the encoded protein. AP2domains within the AP2 transcription factor family may exhibit a higherdegree of sequence homology, such as at least 70% amino acid sequenceidentity including conservative substitutions, and preferably at least80% sequence identity, and more preferably at least 85%, or at leastabout 86%, or at least about 87%, or at least about 88%, or at leastabout 90%, or at least about 95%, or at least about 98% sequenceidentity. Transcription factors that are homologous to the listedsequences should share at least 30%, or at least about 60%, or at leastabout 75%, or at least about 80%, or at least about 90%, or at leastabout 95% amino acid sequence identity over the entire length of thepolypeptide or the homolog.

Percent identity can be determined electronically, for example, by usingthe MEGALIGN program (DNASTAR, Inc. Madison, Wis.). The MEGALIGN programcan create alignments between two or more sequences according todifferent methods, for example, the clustal method (for example, inHiggins and Sharp (1988) Gene 73: 237-244). The clustal algorithm groupssequences into clusters by examining the distances between all pairs.The clusters are aligned pairwise and then in groups. Other alignmentalgorithms or programs may be used, including FASTA, BLAST, or ENTREZ,FASTA and BLAST, and which may be used to calculate percent similarity.These are available as a part of the GCG sequence analysis package(University of Wisconsin, Madison, Wis.), and can be used with orwithout default settings. ENTREZ is available through the NationalCenter for Biotechnology Information. In one embodiment, the percentidentity of two sequences can be determined by the GCG program with agap weight of 1, for example, each amino acid gap is weighted as if itwere a single amino acid or nucleotide mismatch between the twosequences (U.S. Pat. No. 6,262,333).

Other techniques for alignment are described in Methods in Enzymology,vol. 266, Computer Methods for Macromolecular Sequence Analysis (1996),ed. Doolittle, Academic Press, Inc., San Diego, Calif., USA. Preferably,an alignment program that permits gaps in the sequence is utilized toalign the sequences. The Smith-Waterman is one type of algorithm thatpermits gaps in sequence alignments (Shpaer (1997) Methods Mol. Biol.70: 173-187). Also, the GAP program using the Needleman and Wunschalignment method can be utilized to align sequences. An alternativesearch strategy uses MPSRCH software, which runs on a MASPAR computer.MPSRCH uses a Smith-Waterman algorithm to score sequences on a massivelyparallel computer. This approach improves ability to pick up distantlyrelated matches, and is especially tolerant of small gaps and nucleotidesequence errors. Nucleic acid-encoded amino acid sequences can be usedto search both protein and DNA databases.

The percentage similarity between two polypeptide sequences, forexample, sequence A and sequence B, is calculated by dividing the lengthof sequence A, minus the number of gap residues in sequence A, minus thenumber of gap residues in sequence B, into the sum of the residuematches between sequence A and sequence B, times one hundred. Gaps oflow or of no similarity between the two amino acid sequences are notincluded in determining percentage similarity. Percent identity betweenpolynucleotide sequences can also be counted or calculated by othermethods known in the art, for example, the Jotun Hein method (forexample, in Hein (1990) Methods Enzymol. 183: 626-645). Identity betweensequences can also be determined by other methods known in the art, forexample, by varying hybridization conditions (US Patent Application No.20010010913).

Thus, the invention provides methods for identifying a sequence similaror paralogous or orthologous or homologous to one or morepolynucleotides as noted herein, or one or more target polypeptidesencoded by the polynucleotides, or otherwise noted herein and mayinclude linking or associating a given plant phenotype or gene functionwith a sequence. In the methods, a sequence database is provided(locally or across an internet or intranet) and a query is made againstthe sequence database using the relevant sequences herein and associatedplant phenotypes or gene functions.

In addition, one or more polynucleotide sequences or one or morepolypeptides encoded by the polynucleotide sequences may be used tosearch against a BLOCKS (Bairoch et al. (1997) Nucleic Acids Res. 25:217-221), PFAM, and other databases which contain previously identifiedand annotated motifs, sequences and gene functions. Methods that searchfor primary sequence patterns with secondary structure gap penalties(Smith et al. (1992) Protein Engineering 5: 35-51) as well as algorithmssuch as Basic Local Alignment Search Tool (BLAST; Altschul (1993) J.Mol. Evol. 36: 290-300; Altschul et al. (1990) J. Mol. Biol. 215:403-410), BLOCKS (Henikoff and Henikoff (1991) Nucleic Acids Res. 19:6565-6572), Hidden Markov Models (HMM; Eddy (1996) Curr. Opin. Str.Biol. 6: 361-365; Sonnhammer et al. (1997) Proteins 28: 405-420), andthe like, can be used to manipulate and analyze polynucleotide andpolypeptide sequences encoded by polynucleotides. These databases,algorithms and other methods are well known in the art and are describedin Ausubel et al. (1997) Short Protocols in Molecular Biology, JohnWiley & Sons, New York, N.Y., unit 7.7) and in Meyers (1995) MolecularBiology and Biotechnology, Wiley VCH, New York, N.Y., p 856-853).

A further method for identifying or confirming that specific homologoussequences control the same function is by comparison of the transcriptprofile(s) obtained upon overexpression or knockout of two or morerelated transcription factors. Since transcript profiles are diagnosticfor specific cellular states, one skilled in the art will appreciatethat genes that have a highly similar transcript profile (for example,with greater than 50% regulated transcripts in common, more preferablywith greater than 70% regulated transcripts in common, most preferablywith greater than 90% regulated transcripts in common) will have highlysimilar functions. Fowler et al. (2002) Plant Cell 14: 1675-1679) haveshown that three paralogous AP2 family genes (CBF1, CBF2 and CBF3), eachof which is induced upon cold treatment, and each of which can conditionimproved freezing tolerance, have highly similar transcript profiles.Once a transcription factor has been shown to provide a specificfunction, its transcript profile becomes a diagnostic tool to determinewhether putative paralogs or orthologs have the same function.

Furthermore, methods using manual alignment of sequences similar orhomologous to one or more polynucleotide sequences or one or morepolypeptides encoded by the polynucleotide sequences may be used toidentify regions of similarity and AP2 binding domains. Such manualmethods are well-known of those of skill in the art and can include, forexample, comparisons of tertiary structure between a polypeptidesequence encoded by a polynucleotide that comprises a known functionwith a polypeptide sequence encoded by a polynucleotide sequence whichhas a function not yet determined. Such examples of tertiary structuremay comprise predicted α-helices, β-sheets, amphipathic helices, leucinezipper motifs, zinc finger motifs, proline-rich regions, cysteine repeatmotifs, and the like.

Orthologs and paralogs of presently disclosed transcription factors maybe cloned using compositions provided by the present invention accordingto methods well known in the art. cDNAs can be cloned using mRNA from aplant cell or tissue that expresses one of the present transcriptionfactors. Appropriate mRNA sources may be identified by interrogatingNorthern blots with probes designed from the present transcriptionfactor sequences, after which a library is prepared from the mRNAobtained from a positive cell or tissue. Transcription factor-encodingcDNA is then isolated using, for example, PCR, using primers designedfrom a presently disclosed transcription factor gene sequence, or byprobing with a partial or complete cDNA or with one or more sets ofdegenerate probes based on the disclosed sequences. The cDNA library maybe used to transform plant cells. Expression of the cDNAs of interest isdetected using, for example, methods disclosed herein such asmicroarrays, Northern blots, quantitative PCR, or any other techniquefor monitoring changes in expression. Genomic clones may be isolatedusing similar techniques to those.

Identifying Polynucleotides or Nucleic Acids by Hybridization

Polynucleotides homologous to the sequences illustrated in the SequenceListing and tables can be identified, for example, by hybridization toeach other under stringent or under highly stringent conditions.Single-stranded polynucleotides hybridize when they associate based on avariety of well characterized physical-chemical forces, such as hydrogenbonding, solvent exclusion, base stacking and the like. The stringencyof a hybridization reflects the degree of sequence identity of thenucleic acids involved, such that the higher the stringency, the moresimilar are the two polynucleotide strands. Stringency is influenced bya variety of factors, including temperature, salt concentration andcomposition, organic and non-organic additives, solvents, etc. presentin both the hybridization and wash solutions and incubations (and numberthereof), as described in more detail in the references cited above.

Stability of DNA duplexes is affected by such factors as basecomposition, length, and degree of base pair mismatch. Hybridizationconditions may be adjusted to allow DNAs of different sequencerelatedness to hybridize. The melting temperature (T_(m)) is defined asthe temperature when 50% of the duplex molecules have dissociated intotheir constituent single strands. The melting temperature of a perfectlymatched duplex, where the hybridization buffer contains formamide as adenaturing agent, may be estimated by the following equations:

(I) DNA-DNA:

T_(m)(° C.)=81.5+16.6(log [Na+])+0.41(% G+C)−0.62(% formamide)−500/L

(II) DNA-RNA:

T_(m)(° C.)=79.8+18.5(log [Na+])+0.58(% G+C)+0.12(% G+C)²−0.5(%formamide)−820/L

(III) RNA-RNA:

T_(m)(° C.)=79.8+18.5(log [Na+])+0.58(% G+C)+0.12(% G+C)²−0.35(%formamide)−820/L

where L is the length of the duplex formed, [Na+] is the molarconcentration of the sodium ion in the hybridization or washingsolution, and % G+C is the percentage of (guanine+cytosine) bases in thehybrid. For imperfectly matched hybrids, approximately 1° C. is requiredto reduce the melting temperature for each 1% mismatch.

Hybridization experiments are generally conducted in a buffer of pHbetween 6.8 to 7.4, although the rate of hybridization is nearlyindependent of pH at ionic strengths likely to be used in thehybridization buffer (Anderson and Young (1985) “Quantitative FilterHybridisation.” In: Hames and Higgins, ed., Nucleic Acid Hybridisation,A Practical Approach. Oxford, IRL Press, 73-111). In addition, one ormore of the following may be used to reduce non-specific hybridization:sonicated salmon sperm DNA or another non-complementary DNA, bovineserum albumin, sodium pyrophosphate, sodium dodecylsulfate (SDS),polyvinyl-pyrrolidone, ficoll and Denhardt's solution. Dextran sulfateand polyethylene glycol 6000 act to exclude DNA from solution, thusraising the effective probe DNA concentration and the hybridizationsignal within a given unit of time. In some instances, conditions ofeven greater stringency may be desirable or required to reducenon-specific and/or background hybridization. These conditions may becreated with the use of higher temperature, lower ionic strength andhigher concentration of a denaturing agent such as formamide.

Stringency conditions can be adjusted to screen for moderately similarfragments such as homologous sequences from distantly related organisms,or to highly similar fragments such as genes that duplicate functionalenzymes from closely related organisms. The stringency can be adjustedeither during the hybridization step or in the post-hybridizationwashes. Salt concentration, formamide concentration, hybridizationtemperature and probe lengths are variables that can be used to alterstringency (as described by the formula above). As a general guidelineshigh stringency is typically performed at T_(m)−5° C. to T_(m)−20° C.,moderate stringency at T_(m)−20° C. to T_(m)−35° C. and low stringencyat T_(m)−35° C. to T_(m)−50° C. for duplex >150 base pairs.Hybridization may be performed at low to moderate stringency (25-50° C.below T_(m)), followed by post-hybridization washes at increasingstringencies. Maximum rates of hybridization in solution are determinedempirically to occur at T_(m)−25° C. for DNA-DNA duplex and T_(m)−15° C.for RNA-DNA duplex. Optionally, the degree of dissociation may beassessed after each wash step to determine the need for subsequent,higher stringency wash steps.

High stringency conditions may be used to select for nucleic acidsequences with high degrees of identity to the disclosed sequences. Anexample of stringent hybridization conditions obtained in a filter-basedmethod such as a Southern or northern blot for hybridization ofcomplementary nucleic acids that have more than 100 complementaryresidues is about 5° C. to 20° C. lower than the thermal melting point(T_(m)) for the specific sequence at a defined ionic strength and pH.Conditions used for hybridization may include about 0.02 M to about 0.15M sodium chloride, about 0.5% to about 5% casein, about 0.02% SDS orabout 0.1% N-laurylsarcosine, about 0.001 M to about 0.03 M sodiumcitrate, at hybridization temperatures between about 50° C. and about70° C. More preferably, high stringency conditions are about 0.02 Msodium chloride, about 0.5% casein, about 0.02% SDS, about 0.001 Msodium citrate, at a temperature of about 50° C. Nucleic acid moleculesthat hybridize under stringent conditions will typically hybridize to aprobe based on either the entire DNA molecule or selected portions, forexample, to a unique subsequence, of the DNA.

Stringent salt concentration will ordinarily be less than about 750 mMNaCl and 75 mM trisodium citrate. Increasingly stringent conditions maybe obtained with less than about 500 mM NaCl and 50 mM trisodiumcitrate, to even greater stringency with less than about 250 mM NaCl and25 mM trisodium citrate. Low stringency hybridization can be obtained inthe absence of organic solvent, for example, formamide, whereas highstringency hybridization may be obtained in the presence of at leastabout 35% formamide, and more preferably at least about 50% formamide.Stringent temperature conditions will ordinarily include temperatures ofat least about 30° C., more preferably of at least about 37° C., andmost preferably of at least about 42° C. with formamide present. Varyingadditional parameters, such as hybridization time, the concentration ofdetergent, for example, sodium dodecyl sulfate (SDS) and ionic strength,are well known to those skilled in the art. Various levels of stringencyare accomplished by combining these various conditions as needed.

The washing steps that follow hybridization may also vary in stringency;the post-hybridization wash steps primarily determine hybridizationspecificity, with the most critical factors being temperature and theionic strength of the final wash solution. Wash stringency can beincreased by decreasing salt concentration or by increasing temperature.Stringent salt concentration for the wash steps will preferably be lessthan about 30 mM NaCl and 3 mM trisodium citrate, and most preferablyless than about 15 mM NaCl and 1.5 mM trisodium citrate.

Thus, hybridization and wash conditions that may be used to bind andremove polynucleotides with less than the desired homology to thenucleic acid sequences or their complements that encode the presenttranscription factors include, for example:

6×SSC at 65° C.;

50% formamide, 4×SSC at 42° C.; or

0.5×SSC, 0.1% SDS at 65° C.;

with, for example, two wash steps of 10-30 minutes each. Usefulvariations on these conditions will be readily apparent to those skilledin the art.

A person of skill in the art would not expect substantial variationamong polynucleotide species encompassed within the scope of the presentinvention because the highly stringent conditions set forth in the aboveformulae yield structurally similar polynucleotides.

If desired, one may employ wash steps of even greater stringency,including about 0.2×SSC, 0.1% SDS at 65° C. and washing twice, each washstep being about 30 min, or about 0.1×SSC, 0.1% SDS at 65° C. andwashing twice for 30 min. The temperature for the wash solutions willordinarily be at least about 25° C., and for greater stringency at leastabout 42° C. Hybridization stringency may be increased further by usingthe same conditions as in the hybridization steps, with the washtemperature raised about 3° C. to about 5° C., and stringency may beincreased even further by using the same conditions except the washtemperature is raised about 6° C. to about 9° C. For identification ofless closely related homologs, wash steps may be performed at a lowertemperature, for example, 50° C.

An example of a low stringency wash step employs a solution andconditions of at least 25° C. in 30 mM NaCl, 3 mM trisodium citrate, and0.1% SDS over 30 min. Greater stringency may be obtained at 42° C. in 15mM NaCl, with 1.5 mM trisodium citrate, and 0.1% SDS over 30 min. Evenhigher stringency wash conditions are obtained at 65° C.-68° C. in asolution of 15 mM NaCl, 1.5 mM trisodium citrate, and 0.1% SDS. Washprocedures will generally employ at least two final wash steps.Additional variations on these conditions will be readily apparent tothose skilled in the art (for example, in US Patent Application No.20010010913).

Stringency conditions can be selected such that an oligonucleotide thatis perfectly complementary to the coding oligonucleotide hybridizes tothe coding oligonucleotide with at least about a 5-10× higher signal tonoise ratio than the ratio for hybridization of the perfectlycomplementary oligonucleotide to a nucleic acid encoding a transcriptionfactor known as of the filing date of the application. It may bedesirable to select conditions for a particular assay such that a highersignal to noise ratio, that is, about 15× or more, is obtained.Accordingly, a subject nucleic acid will hybridize to a unique codingoligonucleotide with at least a 2× or greater signal to noise ratio ascompared to hybridization of the coding oligonucleotide to a nucleicacid encoding known polypeptide. The particular signal will depend onthe label used in the relevant assay, for example, a fluorescent label,a colorimetric label, a radioactive label, or the like. Labeledhybridization or PCR probes for detecting related polynucleotidesequences may be produced by oligolabeling, nick translation,end-labeling, or PCR amplification using a labeled nucleotide.

Encompassed by the invention are polynucleotide sequences that arecapable of hybridizing to the polynucleotide sequences of the SequenceListing, and fragments thereof under various conditions of stringency(for example, in Wahl and Berger (1987) Methods Enzymol. 152: 399-407,and Kimmel (1987) Methods Enzymol. 152: 507-511). Estimates of homologyare provided by either DNA-DNA or DNA-RNA hybridization under conditionsof stringency as is well understood by those skilled in the art (Hamesand Higgins, Eds. (1985) Nucleic Acid Hybridisation: A PracticalApproach, IRL Press, Oxford, U.K.). Stringency conditions can beadjusted to screen for moderately similar fragments, such as homologoussequences from distantly related organisms, to highly similar fragments,such as genes that duplicate functional enzymes from closely relatedorganisms. Post-hybridization washes determine stringency conditions.

Identifying Polynucleotides or Nucleic Acids with Expression Libraries

In addition to hybridization methods, transcription factor homologpolypeptides can be obtained by screening an expression library usingantibodies specific for one or more transcription factors. With theprovision herein of the disclosed transcription factor, andtranscription factor homolog nucleic acid sequences, the encodedpolypeptide(s) can be expressed and purified in a heterologousexpression system (for example, E. coli) and used to raise antibodies(monoclonal or polyclonal) specific for the polypeptide(s) in question.Antibodies can also be raised against synthetic peptides derived fromthe amino acid sequences or subsequences of a transcription factor ortranscription factor homolog. Methods of raising antibodies are wellknown in the art and are described in Harlow and Lane (1988),Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, NewYork. Such antibodies can then be used to screen an expression libraryproduced from the plant from which it is desired to clone additionaltranscription factor homologs, using the methods described above. Theselected cDNAs can be confirmed by sequencing and enzymatic activity.

Sequence Variations

It will readily be appreciated by those of skill in the art, that any ofa variety of polynucleotide sequences are capable of encoding thetranscription factors and transcription factor homolog polypeptides ofthe invention. Due to the degeneracy of the genetic code, many differentpolynucleotides can encode identical and/or substantially similarpolypeptides in addition to those sequences illustrated in the SequenceListing. Nucleic acids having a sequence that differs from the sequencesshown in the Sequence Listing, or complementary sequences, that encodefunctionally equivalent peptides (i.e., peptides having some degree ofequivalent or similar biological activity) but differ in sequence fromthe sequence shown in the Sequence Listing due to degeneracy in thegenetic code, are also within the scope of the invention.

Altered polynucleotide sequences encoding polypeptides include thosesequences with deletions, insertions, or substitutions of differentnucleotides, resulting in a polynucleotide encoding a polypeptide withat least one functional characteristic of the instant polypeptides.Included within this definition are polymorphisms which may or may notbe readily detectable using a particular oligonucleotide probe of thepolynucleotide encoding the instant polypeptides, and improper orunexpected hybridization to allelic variants, with a locus other thanthe normal chromosomal locus for the polynucleotide sequence encodingthe instant polypeptides.

Allelic variant refers to any of two or more alternative forms of a geneoccupying the same chromosomal locus. Allelic variation arises naturallythrough mutation, and may result in phenotypic polymorphism withinpopulations. Gene mutations can be silent (i.e., no change in theencoded polypeptide) or may encode polypeptides having altered aminoacid sequence. The term allelic variant is also used herein to denote aprotein encoded by an allelic variant of a gene. Splice variant refersto alternative forms of RNA transcribed from a gene. Splice variationarises naturally through use of alternative splicing sites within atranscribed RNA molecule, or less commonly between separatelytranscribed RNA molecules, and may result in several mRNAs transcribedfrom the same gene. Splice variants may encode polypeptides havingaltered amino acid sequence. The term splice variant is also used hereinto denote a protein encoded by a splice variant of an mRNA transcribedfrom a gene.

Those skilled in the art would recognize that, for example, G2133, SEQID NO: 12, represents a single transcription factor; allelic variationand alternative splicing may be expected to occur. Allelic variants ofSEQ ID NO: 11 can be cloned by probing cDNA or genomic libraries fromdifferent individual organisms according to standard procedures. Allelicvariants of the DNA sequence shown in SEQ ID NO: 11, including thosecontaining silent mutations and those in which mutations result in aminoacid sequence changes, are within the scope of the present invention, asare proteins which are allelic variants of SEQ ID NO: 12. cDNAsgenerated from alternatively spliced mRNAs, which retain the propertiesof the transcription factor are included within the scope of the presentinvention, as are polypeptides encoded by such cDNAs and mRNAs. Allelicvariants and splice variants of these sequences can be cloned by probingcDNA or genomic libraries from different individual organisms or tissuesaccording to standard procedures known in the art (U.S. Pat. No.6,388,064).

Thus, in addition to the sequences set forth in the Sequence Listing,the invention also encompasses related nucleic acid molecules thatinclude allelic or splice variants of the sequences of the SequenceListing, and include sequences that are complementary to any of theabove nucleotide sequences. Related nucleic acid molecules also includenucleotide sequences encoding a polypeptide comprising a substitution,modification, addition and/or deletion of one or more amino acidresidues compared to the polypeptide sequences of the Sequence Listingand equivalogs. Such related polypeptides may comprise, for example,additions and/or deletions of one or more N-linked or O-linkedglycosylation sites, or an addition and/or a deletion of one or morecysteine residues.

For example, Table 5 illustrates, for example, that the codons AGC, AGT,TCA, TCC, TCG, and TCT all encode the same amino acid: serine.Accordingly, at each position in the sequence where there is a codonencoding serine, any of the above trinucleotide sequences can be usedwithout altering the encoded polypeptide.

TABLE 5 Amino acid Possible Codons Alanine Ala A GCA GCC GCG GCTCysteine Cys C TGC TGT Aspartic acid Asp D GAC GAT Glutamic acid Glu EGAA GAG Phenylalanine Phe F TTC TTT Glycine Gly G GGA GGC GGG GGTHistidine His H CAC CAT Isoleucine Ile I ATA ATC ATT Lysine Lys KAAA AAG Leucine Leu L TTA TTG CTA CTC CTG CTT Methionine Met M ATGAsparagine Asn N AAC AAT Proline Pro P CCA CCC CCG CCT Glutamine Gln QCAA CAG Arginine Arg R AGA AGG CGA CGC CGG CGT Serine Ser SAGC AGT TCA TCC TCG TCT Threonine Thr T ACA ACC ACG ACT Valine Val VGTA GTC GTG GTT Tryptophan Trp W TGG Tyrosine Tyr Y TAC TAT

Sequence alterations that do not change the amino acid sequence encodedby the polynucleotide are termed “silent” variations. With the exceptionof the codons ATG and TGG, encoding methionine and tryptophan,respectively, any of the possible codons for the same amino acid can besubstituted by a variety of techniques, for example, site-directedmutagenesis, available in the art. Accordingly, any and all suchvariations of a sequence selected from the above table are a feature ofthe invention.

In addition to silent variations, other conservative variations thatalter one, or a few amino acid residues in the encoded polypeptide, canbe made without altering the function of the polypeptide, theseconservative variants are, likewise, a feature of the invention.

For example, substitutions, deletions and insertions introduced into thesequences provided in the Sequence Listing, are also envisioned by theinvention. Such sequence modifications can be engineered into a sequenceby site-directed mutagenesis (Wu (ed.) Methods Enzymol. (1993) vol. 217,Academic Press) or the other methods noted below Amino acidsubstitutions are typically of single residues; insertions usually willbe on the order of about from 1 to 10 amino acid residues; and deletionswill range about from 1 to 30 residues. In one embodiment, deletions orinsertions are made in adjacent pairs, for example, a deletion of tworesidues or insertion of two residues. Substitutions, deletions,insertions or any combination thereof can be combined to arrive at asequence. The mutations that are made in the polynucleotide encoding thetranscription factor should not place the sequence out of reading frameand should not create complementary regions that could produce secondarymRNA structure. Preferably, the polypeptide encoded by the DNA performsthe desired function.

Conservative substitutions are those in which at least one residue inthe amino acid sequence has been removed and a different residueinserted in its place. Such substitutions generally are made inaccordance with the Table 6 when it is desired to maintain the activityof the protein. Table 6 shows amino acids which can be substituted foran amino acid in a protein and which are typically regarded asconservative substitutions.

TABLE 6 Residue Substitutions Conservative Ala Ser Arg Lys Asn Gln; HisAsp Glu Gln Asn Cys Ser Glu Asp Gly Pro His Asn; Gln Ile Leu, Val LeuIle; Val Lys Arg; Gln Met Leu; Ile Phe Met; Leu; Tyr Ser Thr; Gly ThrSer; Val Trp Tyr Tyr Trp; Phe Val Ile; Leu

The polypeptides provided in the Sequence Listing have a novel activity,such as, for example, regulatory activity. Although all conservativeamino acid substitutions (for example, one basic amino acid substitutedfor another basic amino acid) in a polypeptide will not necessarilyresult in the polypeptide retaining its activity, it is expected thatmany of these conservative mutations would result in the polypeptideretaining its activity. Most mutations, conservative ornon-conservative, made to a protein but outside of a conserved domainrequired for function and protein activity will not affect the activityof the protein to any great extent.

Similar substitutions are those in which at least one residue in theamino acid sequence has been removed and a different residue inserted inits place. Such substitutions generally are made in accordance with theTable 7 when it is desired to maintain the activity of the protein.Table 7 shows amino acids which can be substituted for an amino acid ina protein and which are typically regarded as structural and functionalsubstitutions. For example, a residue in column 1 of Table 7 may besubstituted with a residue in column 2; in addition, a residue in column2 of Table 7 may be substituted with the residue of column 1.

TABLE 7 Residue Similar Substitutions Ala Ser; Thr; Gly; Val; Leu; IleArg Lys; His; Gly Asn Gln; His; Gly; Ser; Thr Asp Glu, Ser; Thr Gln Asn;Ala Cys Ser; Gly Glu Asp Gly Pro; Arg His Asn; Gln; Tyr; Phe; Lys; ArgIle Ala; Leu; Val; Gly; Met Leu Ala; Ile; Val; Gly; Met Lys Arg; His;Gln; Gly; Pro Met Leu; Ile; Phe Phe Met; Leu; Tyr; Trp; His; Val; AlaSer Thr; Gly; Asp; Ala; Val; Ile; His Thr Ser; Val; Ala; Gly Trp Tyr;Phe; His Tyr Trp; Phe; His Val Ala; Ile; Leu; Gly; Thr; Ser; Glu

Substitutions that are less conservative than those in Table 7 can beselected by picking residues that differ more significantly in theireffect on maintaining (a) the structure of the polypeptide backbone inthe area of the substitution, for example, as a sheet or helicalconformation, (b) the charge or hydrophobicity of the molecule at thetarget site, or (c) the bulk of the side chain. The substitutions whichin general are expected to produce the greatest changes in proteinproperties will be those in which (a) a hydrophilic residue, forexample, seryl or threonyl, is substituted for (or by) a hydrophobicresidue, for example, leucyl, isoleucyl, phenylalanyl, valyl or alanyl;(b) a cysteine or proline is substituted for (or by) any other residue;(c) a residue having an electropositive side chain, for example, lysyl,arginyl, or histidyl, is substituted for (or by) an electronegativeresidue, for example, glutamyl or aspartyl; or (d) a residue having abulky side chain, for example, phenylalanine, is substituted for (or by)one not having a side chain, for example, glycine.

Further Modifying Sequences of the Invention—Mutation/Forced Evolution

In addition to generating silent or conservative substitutions as noted,above, the present invention optionally includes methods of modifyingthe sequences of the Sequence Listing. In the methods, nucleic acid orprotein modification methods are used to alter the given sequences toproduce new sequences and/or to chemically or enzymatically modify givensequences to change the properties of the nucleic acids or proteins.

Thus, in one embodiment, given nucleic acid sequences are modified, forexample, according to standard mutagenesis or artificial evolutionmethods to produce modified sequences. The modified sequences may becreated using purified natural polynucleotides isolated from anyorganism or may be synthesized from purified compositions and chemicalsusing chemical means well known to those of skill in the art. Forexample, Ausubel, supra, provides additional details on mutagenesismethods. Artificial forced evolution methods are described, for example,by Stemmer (1994) Nature 370: 389-391, Stemmer (1994) Proc. Natl. Acad.Sci. 91: 10747-10751, and U.S. Pat. Nos. 5,811,238, 5,837,500, and6,242,568. Methods for engineering synthetic transcription factors andother polypeptides are described, for example, by Zhang et al. (2000) J.Biol. Chem. 275: 33850-33860, Liu et al. (2001) J. Biol. Chem. 276:11323-11334, and Isalan et al. (2001) Nature Biotechnol. 19: 656-660.Many other mutation and evolution methods are also available andexpected to be within the skill of the practitioner.

Similarly, chemical or enzymatic alteration of expressed nucleic acidsand polypeptides can be performed by standard methods. For example,sequence can be modified by addition of lipids, sugars, peptides,organic or inorganic compounds, by the inclusion of modified nucleotidesor amino acids, or the like. For example, protein modificationtechniques are illustrated in Ausubel, supra. Further details onchemical and enzymatic modifications can be found herein. Thesemodification methods can be used to modify any given sequence, or tomodify any sequence produced by the various mutation and artificialevolution modification methods noted herein.

Accordingly, the invention provides for modification of any givennucleic acid by mutation, evolution, chemical or enzymatic modification,or other available methods, as well as for the products produced bypracticing such methods, for example, using the sequences herein as astarting substrate for the various modification approaches.

For example, optimized coding sequence containing codons preferred by aparticular prokaryotic or eukaryotic host can be used for example, toincrease the rate of translation or to produce recombinant RNAtranscripts having desirable properties, such as a longer half-life, ascompared with transcripts produced using a non-optimized sequence.Translation stop codons can also be modified to reflect host preference.For example, preferred stop codons for Saccharomyces cerevisiae andmammals are TAA and TGA, respectively. The preferred stop codon formonocotyledonous plants is TGA, whereas insects and E. coli prefer touse TAA as the stop codon.

The polynucleotide sequences of the present invention can also beengineered in order to alter a coding sequence for a variety of reasons,including but not limited to, alterations which modify the sequence tofacilitate cloning, processing and/or expression of the gene product.For example, alterations are optionally introduced using techniqueswhich are well known in the art, for example, site-directed mutagenesis,to insert new restriction sites, to alter glycosylation patterns, tochange codon preference, to introduce splice sites, etc.

Furthermore, a fragment or domain derived from any of the polypeptidesof the invention can be combined with domains derived from othertranscription factors or synthetic domains to modify the biologicalactivity of a transcription factor. For instance, a DNA-binding domainderived from a transcription factor of the invention can be combinedwith the activation domain of another transcription factor or with asynthetic activation domain. A transcription activation domain assistsin initiating transcription from a DNA-binding site. Examples includethe transcription activation region of VP16 or GAL4 (Moore et al. (1998)Proc. Natl. Acad. Sci. 95: 376-381; Aoyama et al. (1995) Plant Cell 7:1773-1785), peptides derived from bacterial sequences (Ma and Ptashne(1987) Cell 51: 113-119) and synthetic peptides (Giniger and Ptashne(1987) Nature 330: 670-672).

Expression and Modification of Polypeptides

Typically, polynucleotide sequences of the invention are incorporatedinto recombinant DNA (or RNA) molecules that direct expression ofpolypeptides of the invention in appropriate host cells, transgenicplants, in vitro translation systems, or the like. Due to the inherentdegeneracy of the genetic code, nucleic acid sequences which encodesubstantially the same or a functionally equivalent amino acid sequencecan be substituted for any listed sequence to provide for cloning andexpressing the relevant homolog.

The transgenic plants of the present invention comprising recombinantpolynucleotide sequences are generally derived from parental plants,which may themselves be non-transformed (or non-transgenic) plants.These transgenic plants may either have a transcription factor gene“knocked out” (for example, with a genomic insertion by homologousrecombination, an antisense or ribozyme construct) or expressed to anormal or wild-type extent. However, overexpressing transgenic “progeny”plants will exhibit greater mRNA levels, wherein the mRNA encodes atranscription factor, that is, a DNA-binding protein that is capable ofbinding to a DNA regulatory sequence and inducing transcription, andpreferably, expression of a plant trait gene. Preferably, the mRNAexpression level will be at least three-fold greater than that of theparental plant, or more preferably at least ten-fold greater mRNA levelscompared to said parental plant, and most preferably at least fifty-foldgreater compared to said parental plant.

Vectors, Promoters, and Expression Systems

The present invention includes recombinant constructs comprising one ormore of the nucleic acid sequences herein. The constructs typicallycomprise a vector, such as a plasmid, a cosmid, a phage, a virus (forexample, a plant virus), a bacterial artificial chromosome (BAC), ayeast artificial chromosome (YAC), or the like, into which a nucleicacid sequence of the invention has been inserted, in a forward orreverse orientation. In a preferred aspect of this embodiment, theconstruct further comprises regulatory sequences, including, forexample, a promoter, operably linked to the sequence. Large numbers ofsuitable vectors and promoters are known to those of skill in the art,and are commercially available.

General texts that describe molecular biological techniques usefulherein, including the use and production of vectors, promoters and manyother relevant topics, include Berger, Sambrook, supra and Ausubel,supra. Any of the identified sequences can be incorporated into acassette or vector, for example, for expression in plants. A number ofexpression vectors suitable for stable transformation of plant cells orfor the establishment of transgenic plants have been described includingthose described in Weissbach and Weissbach (1989) Methods for PlantMolecular Biology, Academic Press, and Gelvin et al. (1990) PlantMolecular Biology Manual, Kluwer Academic Publishers. Specific examplesinclude those derived from a Ti plasmid of Agrobacterium tumefaciens, aswell as those disclosed by Herrera-Estrella et al. (1983) Nature 303:209, Bevan (1984) Nucleic Acids Res. 12: 8711-8721, Klee (1985)Bio/Technology 3: 637-642, for dicotyledonous plants.

Alternatively, non-Ti vectors can be used to transfer the DNA intomonocotyledonous plants and cells by using free DNA delivery techniques.Such methods can involve, for example, the use of liposomes,electroporation, microprojectile bombardment, silicon carbide whiskers,and viruses. By using these methods transgenic plants such as wheat,rice (Christou (1991) Bio/Technology 9: 957-962) and corn (Gordon-Kamm(1990) Plant Cell 2: 603-618) can be produced. An immature embryo canalso be a good target tissue for monocots for direct DNA deliverytechniques by using the particle gun (Weeks et al. (1993) Plant Physiol.102: 1077-1084; Vasil (1993) Bio/Technology 10: 667-674; Wan and Lemeaux(1994) Plant Physiol. 104: 37-48, and for Agrobacterium-mediated DNAtransfer (Ishida et al. (1996) Nature Biotechnol. 14: 745-750).

Typically, plant transformation vectors include one or more cloned plantcoding sequence (genomic or cDNA) under the transcriptional control of5′ and 3′ regulatory sequences and a dominant selectable marker. Suchplant transformation vectors typically also contain a promoter (forexample, a regulatory region controlling inducible or constitutive,environmentally- or developmentally-regulated, or cell- ortissue-specific expression), a transcription initiation start site, anRNA processing signal (such as intron splice sites), a transcriptiontermination site, and/or a polyadenylation signal.

A potential utility for the transcription factor polynucleotidesdisclosed herein is the isolation of promoter elements from these genesthat can be used to program expression in plants of any genes. Eachtranscription factor gene disclosed herein is expressed in a uniquefashion, as determined by promoter elements located upstream of thestart of translation, and additionally within an intron of thetranscription factor gene or downstream of the termination codon of thegene. As is well known in the art, for a significant portion of genes,the promoter sequences are located entirely in the region directlyupstream of the start of translation. In such cases, typically thepromoter sequences are located within 2.0 kb of the start oftranslation, or within 1.5 kb of the start of translation, frequentlywithin 1.0 kb of the start of translation, and sometimes within 0.5 kbof the start of translation.

The promoter sequences can be isolated according to methods known to oneskilled in the art.

Examples of constitutive plant promoters which can be useful forexpressing the TF sequence include: the cauliflower mosaic virus (CaMV)35S promoter, which confers constitutive, high-level expression in mostplant tissues (for example, in Odell et al. (1985) Nature 313: 810-812);the nopaline synthase promoter (An et al. (1988) Plant Physiol. 88:547-552); and the octopine synthase promoter (Fromm et al. (1989) PlantCell 1: 977-984).

The transcription factors of the invention may be operably linked with aspecific promoter that causes the transcription factor to be expressedin response to environmental, tissue-specific or temporal signals. Avariety of plant gene promoters that regulate gene expression inresponse to environmental, hormonal, chemical, developmental signals,and in a tissue-active manner can be used for expression of a TFsequence in plants. Choice of a promoter is based largely on thephenotype of interest and is determined by such factors as tissue (forexample, seed, fruit, root, pollen, vascular tissue, flower, carpel,etc.), inducibility (for example, in response to wounding, heat, cold,drought, light, pathogens, etc.), timing, developmental stage, and thelike. Numerous known promoters have been characterized and can favorablybe employed to promote expression of a polynucleotide of the inventionin a transgenic plant or cell of interest. For example, tissue-specificpromoters include: seed-specific promoters (such as the napin, phaseolinor DC3 promoter described in U.S. Pat. No. 5,773,697), fruit-specificpromoters that are active during fruit ripening (such as the dru 1promoter (U.S. Pat. No. 5,783,393), or the 2A11 promoter (U.S. Pat. No.4,943,674) and the tomato polygalacturonase promoter (Bird et al. (1988)Plant Mol. Biol. 11: 651-662), root-specific promoters, such as thosedisclosed in U.S. Pat. Nos. 5,618,988, 5,837,848 and 5,905,186,pollen-active promoters such as PTA29, PTA26 and PTA13 (U.S. Pat. No.5,792,929), promoters active in vascular tissue (Ringli and Keller(1998) Plant Mol. Biol. 37: 977-988), flower-specific (Kaiser et al.(1995) Plant Mol. Biol. 28: 231-243), pollen (Baerson et al. (1994)Plant Mol. Biol. 26: 1947-1959), carpels (Ohl et al. (1990) Plant Cell2: 837-848), pollen and ovules (Baerson et al. (1993) Plant Mol. Biol.22: 255-267), auxin-inducible promoters (such as that described in vander Kop et al. (1999) Plant Mol. Biol. 39: 979-990 or Baumann et al.,(1999) Plant Cell 11: 323-334), cytokinin-inducible promoter(Guevara-Garcia (1998) Plant Mol. Biol. 38: 743-753), promotersresponsive to gibberellin (Shi et al. (1998) Plant Mol. Biol. 38:1053-1060, Willmott et al. (1998) Plant Molec. Biol. 38: 817-825) andthe like. Additional promoters are those that elicit expression inresponse to heat (Ainley et al. (1993) Plant Mol. Biol. 22: 13-23),light (for example, the pea rbcS-3A promoter, Kuhlemeier et al. (1989)Plant Cell 1: 471-478), and the maize rbcS promoter, Schaffner and Sheen(1991) Plant Cell 3: 997-1012); wounding (for example, wunI, Siebertz etal. (1989) Plant Cell 1: 961-968); pathogens (such as the PR-1 promoterdescribed in Buchel et al. (1999) Plant Mol. Biol. 40: 387-396, and thePDF1.2 promoter described in Manners et al. (1998) Plant Mol. Biol. 38:1071-1080), and chemicals such as methyl jasmonate or salicylic acid(Gatz (1997) Annu. Rev. Plant Physiol. Plant Mol. Biol. 48: 89-108). Inaddition, the timing of the expression can be controlled by usingpromoters such as those acting at senescence (Gan and Amasino (1995)Science 270: 1986-1988); or late seed development (Odell et al. (1994)Plant Physiol. 106: 447-458).

Plant expression vectors can also include RNA processing signals thatcan be positioned within, upstream or downstream of the coding sequence.In addition, the expression vectors can include additional regulatorysequences from the 3′-untranslated region of plant genes, for example, a3′ terminator region to increase mRNA stability of the mRNA, such as thePI-II terminator region of potato or the octopine or nopaline synthase3′ terminator regions.

Additional Expression Elements

Specific initiation signals can aid in efficient translation of codingsequences. These signals can include, for example, the ATG initiationcodon and adjacent sequences. No additional translational controlsignals may be needed where a coding sequence, its initiation codon andupstream sequences are inserted into the appropriate expression vector.However, in cases where only coding sequence (for example, a matureprotein coding sequence) or a portion thereof is inserted, exogenoustranscriptional control signals including the ATG initiation codon canbe separately provided. The initiation codon is provided in the correctreading frame to facilitate transcription. Exogenous transcriptionalelements and initiation codons can be of various origins, both naturaland synthetic. The efficiency of expression can be enhanced by theinclusion of enhancers appropriate to the cell system in use.

Expression Hosts

The present invention also relates to host cells which are transducedwith vectors of the invention, and the production of polypeptides of theinvention (including fragments thereof) by recombinant techniques. Hostcells are genetically engineered (i.e., nucleic acids are introduced,for example, transduced, transformed or transfected) with the vectors ofthis invention, which may be, for example, a cloning vector or anexpression vector comprising the relevant nucleic acids herein. Thevector is optionally a plasmid, a viral particle, a phage, a nakednucleic acid, etc. The engineered host cells can be cultured inconventional nutrient media modified as appropriate for activatingpromoters, selecting transformants, or amplifying the relevant gene. Theculture conditions, such as temperature, pH and the like, are thosepreviously used with the host cell selected for expression, and will beapparent to those skilled in the art and in the references cited herein,including, Sambrook, supra and Ausubel, supra.

The host cell can be a eukaryotic cell, such as a yeast cell, or a plantcell, or the host cell can be a prokaryotic cell, such as a bacterialcell. Plant protoplasts are also suitable for some applications. Forexample, the DNA fragments are introduced into plant tissues, culturedplant cells or plant protoplasts by standard methods includingelectroporation (Fromm et al. (1985) Proc. Natl. Acad. Sci. 82:5824-5828), infection by viral vectors such as cauliflower mosaic virus(CaMV) (Hohn et al. (1982) Molecular Biology of Plant Tumors AcademicPress, New York, N.Y., pp. 549-560; U.S. Pat. No. 4,407,956), highvelocity ballistic penetration by small particles with the nucleic acideither within the matrix of small beads or particles, or on the surface(Klein et al. (1987) Nature 327: 70-73), use of pollen as vector (WO85/01856), or use of Agrobacterium tumefaciens or A. rhizogenes carryinga T-DNA plasmid in which DNA fragments are cloned. The T-DNA plasmid istransmitted to plant cells upon infection by Agrobacterium tumefaciens,and a portion is stably integrated into the plant genome (Horsch et al.(1984) Science 233: 496-498; Fraley et al. (1983) Proc. Natl. Acad. Sci.80: 4803-4807).

The cell can include a nucleic acid of the invention that encodes apolypeptide, wherein the cell expresses a polypeptide of the invention.The cell can also include vector sequences, or the like. Furthermore,cells and transgenic plants that include any polypeptide or nucleic acidabove or throughout this specification, for example, produced bytransduction of a vector of the invention, are an additional feature ofthe invention.

For long-term, high-yield production of recombinant proteins, stableexpression can be used. Host cells transformed with a nucleotidesequence encoding a polypeptide of the invention are optionally culturedunder conditions suitable for the expression and recovery of the encodedprotein from cell culture. The protein or fragment thereof produced by arecombinant cell may be secreted, membrane-bound, or containedintracellularly, depending on the sequence and/or the vector used. Aswill be understood by those of skill in the art, expression vectorscontaining polynucleotides encoding mature proteins of the invention canbe designed with signal sequences which direct secretion of the maturepolypeptides through a prokaryotic or eukaryotic cell membrane.

Modified Amino Acid Residues

Polypeptides of the invention may contain one or more modified aminoacid residues. The presence of modified amino acids may be advantageousin, for example, increasing polypeptide half-life, reducing polypeptideantigenicity or toxicity, increasing polypeptide storage stability, orthe like. Amino acid residue(s) are modified, for example,co-translationally or post-translationally during recombinant productionor modified by synthetic or chemical means.

Non-limiting examples of a modified amino acid residue includeincorporation or other use of acetylated amino acids, glycosylated aminoacids, sulfated amino acids, prenylated (for example, farnesylated,geranylgeranylated) amino acids, PEG modified (for example, “PEGylated”)amino acids, biotinylated amino acids, carboxylated amino acids,phosphorylated amino acids, etc. References adequate to guide one ofskill in the modification of amino acid residues are replete throughoutthe literature.

The modified amino acid residues may prevent or increase affinity of thepolypeptide for another molecule, including, but not limited to,polynucleotide, proteins, carbohydrates, lipids and lipid derivatives,and other organic or synthetic compounds.

Identification of Additional Protein Factors

A transcription factor provided by the present invention can also beused to identify additional endogenous or exogenous molecules that canaffect a phenotype or trait of interest. Such molecules includeendogenous molecules that are acted upon either at a transcriptionallevel by a transcription factor of the invention to modify a phenotypeas desired. For example, the transcription factors can be employed toidentify one or more downstream genes that are subject to a regulatoryeffect of the transcription factor. In one approach, a transcriptionfactor or transcription factor homolog of the invention is expressed ina host cell, for example, a transgenic plant cell, tissue or explant,and expression products, either RNA or protein, of likely or randomtargets are monitored, for example, by hybridization to a microarray ofnucleic acid probes corresponding to genes expressed in a tissue or celltype of interest, by two-dimensional gel electrophoresis of proteinproducts, or by any other method known in the art for assessingexpression of gene products at the level of RNA or protein.Alternatively, a transcription factor of the invention can be used toidentify promoter sequences (such as binding sites on DNA sequences)involved in the regulation of a downstream target. After identifying apromoter sequence, interactions between the transcription factor and thepromoter sequence can be modified by changing specific nucleotides inthe promoter sequence or specific amino acids in the transcriptionfactor that interact with the promoter sequence to alter a plant trait.Typically, transcription factor DNA-binding sites are identified by gelshift assays. After identifying the promoter regions, the promoterregion sequences can be employed in double-stranded DNA arrays toidentify molecules that affect the interactions of the transcriptionfactors with their promoters (Bulyk et al. (1999) Nature Biotechnol. 17:573-577).

The identified transcription factors are also useful to identifyproteins that modify the activity of the transcription factor. Suchmodification can occur by covalent modification, such as byphosphorylation, or by protein-protein (homo or -heteropolymer)interactions. Any method suitable for detecting protein-proteininteractions can be employed. Among the methods that can be employed areco-immunoprecipitation, cross-linking and co-purification throughgradients or chromatographic columns, and the two-hybrid yeast system.

The two-hybrid system detects protein interactions in vivo and isdescribed in Chien et al. ((1991) Proc. Natl. Acad. Sci. 88: 9578-9582)and is commercially available from Clontech (Palo Alto, Calif.). In sucha system, plasmids are constructed that encode two hybrid proteins: oneconsists of the DNA-binding domain of a transcription activator proteinfused to the TF polypeptide and the other consists of the transcriptionactivator protein's activation domain fused to an unknown protein thatis encoded by a cDNA that has been recombined into the plasmid as partof a cDNA library. The DNA-binding domain fusion plasmid and the cDNAlibrary are transformed into a strain of the yeast Saccharomycescerevisiae that contains a reporter gene (for example, lacZ) whoseregulatory region contains the transcription activator's binding site.Either hybrid protein alone cannot activate transcription of thereporter gene. Interaction of the two hybrid proteins reconstitutes thefunctional activator protein and results in expression of the reportergene, which is detected by an assay for the reporter gene product. Then,the library plasmids responsible for reporter gene expression areisolated and sequenced to identify the proteins encoded by the libraryplasmids. After identifying proteins that interact with thetranscription factors, assays for compounds that interfere with the TFprotein-protein interactions can be performed.

Subsequences

Also contemplated are uses of polynucleotides, also referred to hereinas oligonucleotides, typically having at least 12 or more bases that hhybridize under stringent or highly stringent conditions to apolynucleotide sequence described above. The polynucleotides may be usedas probes, primers, sense and antisense agents, and the like, accordingto methods as noted above.

Subsequences of the polynucleotides of the invention, includingpolynucleotide fragments and oligonucleotides are useful as nucleic acidprobes and primers. An oligonucleotide suitable for use as a probe orprimer is at least about 15 nucleotides in length, more often at leastabout 18 nucleotides, often at least about 21 nucleotides, frequently atleast about 30 nucleotides, or about 40 nucleotides, or more in length.A nucleic acid probe is useful in hybridization protocols, for example,to identify additional polypeptide homologs of the invention, includingprotocols for microarray experiments. Primers can be annealed to acomplementary target DNA strand by nucleic acid hybridization to form ahybrid between the primer and the target DNA strand, and then extendedalong the target DNA strand by a DNA polymerase enzyme. Primer pairs canbe used for amplification of a nucleic acid sequence, for example, bythe polymerase chain reaction (PCR) or other nucleic-acid amplificationmethods (Sambrook, supra, and Ausubel, supra).

In addition, the invention includes an isolated or recombinantpolypeptide including a subsequence of at least about 15 contiguousamino acids encoded by the recombinant or isolated polynucleotides ofthe invention. For example, such polypeptides, or domains or fragmentsthereof, can be used as immunogens, for example, to produce antibodiesspecific for the polypeptide sequence, or as probes for detecting asequence of interest. A subsequence can range in size from about 15amino acids in length up to and including the full length of thepolypeptide.

To be encompassed by the present invention, an expressed polypeptidewhich comprises such a polypeptide subsequence performs at least onebiological function of the intact polypeptide in substantially the samemanner, or to a similar extent, as does the intact polypeptide. Forexample, a polypeptide fragment can comprise a recognizable structuralmotif or functional domain such as a DNA binding domain that activatestranscription, for example, by binding to a specific DNA promoter regionan activation domain, or a domain for protein-protein interactions.

Production of Transgenic Plants and Modification of Traits.

The polynucleotides of the invention are favorably employed to producetransgenic plants with various traits or characteristics that have beenmodified in a desirable manner, for example, to improve the seedcharacteristics of a plant. For example, alteration of expression levelsor patterns (for example, spatial or temporal expression patterns) ofone or more of the transcription factors (or transcription factorhomologs) of the invention, as compared with the levels of the sameprotein found in a wild-type plant, can be used to modify a plant'straits. An illustrative example of trait modification, improvedcharacteristics, by altering expression levels of a particulartranscription factor is described further in the Examples and theSequence Listing.

Arabidopsis as a Model System.

Arabidopsis thaliana is the object of rapidly growing attention as amodel for genetics and metabolism in plants. Arabidopsis has a smallgenome, and well-documented studies are available. It is easy to grow inlarge numbers and mutants defining important genetically controlledmechanisms are either available, or can readily be obtained. Variousmethods to introduce and express isolated homologous genes are available(Koncz et al., eds., Methods in Arabidopsis Research (1992) WorldScientific, New Jersey, N.J., in “Preface”). Because of its small size,short life cycle, obligate autogamy and high fertility, Arabidopsis isalso a choice organism for the isolation of mutants and studies inmorphogenetic and development pathways, and control of these pathways bytranscription factors (Koncz (1992) supra, p. 72). A number of studiesintroducing transcription factors into A. thaliana have demonstrated theutility of this plant for understanding the mechanisms of generegulation and trait alteration in plants (for example, in Koncz (1992)supra, and in U.S. Pat. No. 6,417,428).

Arabidopsis Genes in Transgenic Plants.

Expression of genes which encode transcription factors modify expressionof endogenous genes, polynucleotides, and proteins are well known in theart. In addition, transgenic plants comprising isolated polynucleotidesencoding transcription factors may also modify expression of endogenousgenes, polynucleotides, and proteins. Examples include Peng et al.(1997) Genes and Development 11: 3194-3205 and Peng et al. (1999) Nature400: 256-261. In addition, many others have demonstrated that anArabidopsis transcription factor expressed in an exogenous plant specieselicits the same or very similar phenotypic response (Fu et al. (2001)Plant Cell 13: 1791-1802; Nandi et al. (2000) Curr. Biol. 10: 215-218;Coupland (1995) Nature 377: 482-483; and Weigel and Nilsson (1995)Nature 377: 482-500.

Homologous Genes Introduced into Transgenic Plants.

Homologous genes that may be derived from any plant, or from any sourcewhether natural, synthetic, semi-synthetic or recombinant, and thatshare significant sequence identity or similarity to those provided bythe present invention, may be introduced into plants, for example, cropplants, to confer desirable or improved traits. Consequently, transgenicplants may be produced that comprise a recombinant expression vector orcassette with a promoter operably linked to one or more sequenceshomologous to presently disclosed sequences. The promoter may be, forexample, a plant or viral promoter.

The invention thus provides for methods for preparing transgenic plants,and for modifying plant traits. These methods include introducing into aplant a recombinant expression vector or cassette comprising afunctional promoter operably linked to one or more sequences homologousto presently disclosed sequences. Plants and kits for producing theseplants that result from the application of these methods are alsoencompassed by the present invention.

Transcription Factors of Interest for the Modification of Plant Traits.

Currently, the existence of a series of maturity groups for differentlatitudes represents a major barrier to the introduction of new valuabletraits. Any trait (for example disease resistance) has to be bred intoeach of the different maturity groups separately, a laborious and costlyexercise. The availability of single strain, which could be grown at anylatitude, would therefore greatly increase the potential for introducingnew traits to crop species such as soybean and cotton.

For the specific effects, traits and utilities conferred to plants, oneor more transcription factor genes of the present invention may be usedto increase or decrease, or improve or prove deleterious to a giventrait. For example, knocking out a transcription factor gene thatnaturally occurs in a plant, or suppressing the gene (with, for example,antisense suppression), may cause decreased tolerance to shade or adrought stress relative to non-transformed or wild-type plants. Byoverexpressing this gene, the plant may experience increased toleranceto the same stress. More than one transcription factor gene may beintroduced into a plant, either by transforming the plant with one ormore vectors comprising two or more transcription factors, or byselective breeding of plants to yield hybrid crosses that comprise morethan one introduced transcription factor.

Genes, Traits and Utilities that Affect Plant Characteristics.

Plant transcription factors can modulate gene expression, and, in turn,be modulated by the environmental experience of a plant. Significantalterations in a plant's environment invariably result in a change inthe plant's transcription factor gene expression pattern. Alteredtranscription factor expression patterns generally result in phenotypicchanges in the plant. Transcription factor gene product(s) in transgenicplants then differ(s) in amounts or proportions from that found inwild-type or non-transformed plants, and those transcription factorslikely represent polypeptides that are used to alter the response to theenvironmental change. By way of example, it is well accepted in the artthat analytical methods based on altered expression patterns may be usedto screen for phenotypic changes in a plant far more effectively thancan be achieved using traditional methods.

Potential Applications of Presently Disclosed Sequences that RegulateAbiotic Stress Tolerance Sugar Sensing.

In addition to their important role as an energy source and structuralcomponent of the plant cell, sugars are central regulatory moleculesthat control several aspects of plant physiology, metabolism anddevelopment (Hsieh et al. (1998) Proc. Natl. Acad. Sci. 95:13965-13970). It is thought that this control is achieved by regulatinggene expression and, in higher plants, sugars have been shown to repressor activate plant genes involved in many essential processes such asphotosynthesis, glyoxylate metabolism, respiration, starch and sucrosesynthesis and degradation, pathogen response, wounding response, cellcycle regulation, pigmentation, flowering and senescence. The mechanismsby which sugars control gene expression are not understood.

Several sugar sensing mutants have turned out to be allelic to ABA andethylene mutants. ABA is found in all photosynthetic organisms and actsas a key regulator of transpiration, stress responses, embryogenesis,and seed germination. Most ABA effects are related to the compoundacting as a signal of decreased water availability, whereby it triggersa reduction in water loss, slows growth, and mediates adaptiveresponses. However, ABA also influences plant growth and development viainteractions with other phytohormones. Physiological and molecularstudies indicate that maize and Arabidopsis have almost identicalpathways with regard to ABA biosynthesis and signal transduction (forexample, in Finkelstein and Rock (2002) “Abscisic acid biosynthesis andresponse”, in The Arabidopsis Book, Somerville and Meyerowitz, editors(American Society of Plant Biologists, Rockville, Md.).

This potentially implicates the sequences of the invention that, whenoverexpressed, confer a sugar sensing or hormone signaling phenotype inplants. On the other hand, the sucrose treatment used in theseexperiments (9.4% w/v) could also be an osmotic stress. Therefore, onecould interpret these data as an indication that these transgenic linesare more tolerant to osmotic stress. However, it is well known thatplant responses to ABA, osmotic and other stress may be linked, andthese different treatments may even act in a synergistic manner toincrease the degree of a response. For example, Xiong, Ishitani, and Zhu((1999) Plant Physiol. 119: 205-212) have shown that genetic andmolecular studies may be used to show extensive interaction betweenosmotic stress, temperature stress, and ABA responses in plants. Theseinvestigators analyzed the expression of RD29A-LUC in response tovarious treatment regimes in Arabidopsis. The RD29A promoter containsboth the ABA-responsive and the dehydration-responsive element—alsotermed the C-repeat—and can be activated by osmotic stress, lowtemperature, or ABA treatment; transcription of the RD29A gene inresponse to osmotic and cold stresses is mediated by both ABA-dependentand ABA-independent pathways (Xiong, Ishitani, and Zhu (1999) supra).LUC refers to the firefly luciferase coding sequence, which, in thiscase, was driven by the stress responsive RD29A promoter. The resultsrevealed both positive and negative interactions, depending on thenature and duration of the treatments. Low temperature stress was foundto impair osmotic signaling but moderate heat stress strongly enhancedosmotic stress induction, thus acting synergistically with osmoticsignaling pathways. In this study, the authors reported that osmoticstress and ABA can act synergistically by showing that the treatmentssimultaneously induced transgene and endogenous gene expression. Similarresults were reported by Bostock and Quatrano ((1992) Plant Physiol. 98:1356-1363), who found that osmotic stress and ABA act synergisticallyand induce maize Em gene expression. Ishitani et al (1997) Plant Cell 9:1935-1949) isolated a group of Arabidopsis single-gene mutations thatconfer enhanced responses to both osmotic stress and ABA. The nature ofthe recovery of these mutants from osmotic stress and ABA treatmentsuggested that although separate signaling pathways exist for osmoticstress and ABA, the pathways share a number of components; these commoncomponents may mediate synergistic interactions between osmotic stressand ABA. Thus, contrary to the previously-held belief that ABA-dependentand ABA-independent stress signaling pathways act in a parallel manner,our data reveal that these pathways cross-talk and converge to activatestress gene expression.

Because sugars are important signaling molecules, the ability to controleither the concentration of a signaling sugar or how the plant perceivesor responds to a signaling sugar could be used to control plantdevelopment, physiology or metabolism. For example, the flux of sucrose(a disaccharide sugar used for systemically transporting carbon andenergy in most plants) has been shown to affect gene expression andalter storage compound accumulation in seeds. Manipulation of thesucrose signaling pathway in seeds may therefore cause seeds to havemore protein, oil or carbohydrate, depending on the type ofmanipulation. Similarly, in tubers, sucrose is converted to starch whichis used as an energy store. It is thought that sugar signaling pathwaysmay partially determine the levels of starch synthesized in the tubers.The manipulation of sugar signaling in tubers could lead to tubers witha higher starch content.

Thus, altering the expression of the presently disclosed transcriptionfactor genes that manipulate the sugar signal transduction pathway,including, for example, G175, G303, G354, G481, G916, G922, G1069,G1073, G1820, G2053, G2701, G2789, G2839, G2854, along with theirequivalogs, or that exhibit an osmotic stress phenotype, including, forexample, G47, G482, G489 or G1069, G1073, as evidenced by theirtolerance to, for example, high mannitol, salt or PEG, may be used toproduce plants with desirable traits, including increased droughttolerance. In particular, manipulation of sugar signal transductionpathways could be used to alter source-sink relationships in seeds,tubers, roots and other storage organs leading to increase in yield.

Abiotic Stress: Drought and Low Humidity Tolerance.

Exposure to dehydration invokes similar survival strategies in plants asdoes freezing stress (for example, in Yelenosky (1989) Plant Physiol 89:444-451) and drought stress induces freezing tolerance (for example, inSiminovitch et al. (1982) Plant Physiol 69: 250-255; and Guy et al.(1992) Planta 188: 265-270). In addition to the induction ofcold-acclimation proteins, strategies that allow plants to survive inlow water conditions may include, for example, reduced surface area, orsurface oil or wax production. Modifying the expression of the presentlydisclosed transcription factor genes, including G2133, G1274, G922,G2999, G3086, G354, G1792, G2053, G975, G1069, G916, G1820, G2701, G47,G2854, G2789, G634, G175, G2839, G1452, G3083, G489, G303, G2992, andG682, and their equivalogs, may be used to increase a plant's toleranceto low water conditions and provide the benefits of improved survival,increased yield and an extended geographic and temporal planting range.

Osmotic Stress.

Modification of the expression of a number of presently disclosedtranscription factor genes, for example, G47, G482, G489 or G1069, G2053and their equivalogs, may be used to increase germination rate or growthunder adverse osmotic conditions, which could impact survival and yieldof seeds and plants. Osmotic stresses may be regulated by specificmolecular control mechanisms that include genes controlling water andion movements, functional and structural stress-induced proteins, signalperception and transduction, and free radical scavenging, and manyothers (Wang et al. (2001) Acta Hort. (ISHS) 560: 285-292). Instigatorsof osmotic stress include freezing, drought and high salinity, each ofwhich are discussed in more detail below.

In many ways, freezing, high salt and drought have similar effects onplants, not the least of which is the induction of common polypeptidesthat respond to these different stresses. For example, freezing issimilar to water deficit in that freezing reduces the amount of wateravailable to a plant. Exposure to freezing temperatures may lead tocellular dehydration as water leaves cells and forms ice crystals inintercellular spaces (Buchanan et al. (2000) in Biochemistry andMolecular Biology of Plants, American Society of Plant Physiologists,Rockville, Md.). As with high salt concentration and freezing, theproblems for plants caused by low water availability include mechanicalstresses caused by the withdrawal of cellular water. Thus, theincorporation of transcription factors that modify a plant's response toosmotic stress into, for example, a crop or ornamental plant, may beuseful in reducing damage or loss. Specific effects caused by freezing,high salt and drought are addressed below.

The Relationship Between Salt, Drought and Freezing Tolerance.

Plants are subject to a range of environmental challenges. Several ofthese, including drought stress, have the ability to impact whole plantand cellular water availability. Not surprisingly, then, plant responsesto this collection of stresses are related. In a recent review, Zhunotes that “most studies on water stress signaling have focused on saltstress primarily because plant responses to salt and drought are closelyrelated and the mechanisms overlap” (Zhu (2002) Ann. Rev. Plant Biol.53: 247-273). Many examples of similar responses and pathways to thisset of stresses have been documented. For example, the CBF transcriptionfactors have been shown to condition resistance to salt, freezing anddrought (Kasuga et al. (1999) Nature Biotech. 17: 287-291). TheArabidopsis rd29B gene is induced in response to both salt anddehydration stress, a process that is mediated largely through an ABAsignal transduction process (Uno et al. (2000) Proc. Natl. Acad. Sci.USA 97: 11632-11637), resulting in altered activity of transcriptionfactors that bind to an upstream element within the rd29B promoter. InMesembryanthemum crystallinum (ice plant), Patharker and Cushman haveshown that a calcium-dependent protein kinase (McCDPK1) is induced byexposure to both drought and salt stresses (Patharker and Cushman (2000)Plant J. 24: 679-691). The stress-induced kinase was also shown tophosphorylate a transcription factor, presumably altering its activity,although transcript levels of the target transcription factor are notaltered in response to salt or drought stress. Similarly, Saijo et al.demonstrated that a rice salt/drought-induced calmodulin-dependentprotein kinase (OsCDPK7) conferred increased salt and drought toleranceto rice when overexpressed (Saijo et al. (2000) Plant J. 23: 319-327).

Exposure to dehydration invokes similar survival strategies in plants asdoes freezing stress (for example, in Yelenosky (1989) Plant Physiol 89:444-451) and drought stress induces freezing tolerance (for example, inSiminovitch et al. (1982) Plant Physiol 69: 250-255; and Guy et al.(1992) Planta 188: 265-270). In addition to the induction ofcold-acclimation proteins, strategies that allow plants to survive inlow water conditions may include, for example, reduced surface area, orsurface oil or wax production.

Consequently, one skilled in the art would expect that some pathwaysinvolved in resistance to one of these stresses, and hence regulated byan individual transcription factor, will also be involved in resistanceto another of these stresses, regulated by the same or homologoustranscription factors. Of course, the overall resistance pathways arerelated, not identical, and therefore not all transcription factorscontrolling resistance to one stress will control resistance to theother stresses. Nonetheless, if a transcription factor conditionsresistance to one of these stresses, it would be apparent to one skilledin the art to test for resistance to these related stresses.

Thus, the genes of the sequence listing, including, for example, G175,G922, G1452, G1820, G2701, G2999, G3086 and their equivalogs thatprovide tolerance to salt may be used to engineer salt tolerant cropsand trees that can flourish in soils with high saline content or underdrought conditions. In particular, increased salt tolerance during thegermination stage of a plant enhances survival and yield. Presentlydisclosed transcription factor genes that provide increased salttolerance during germination, the seedling stage, and throughout aplant's life cycle, would find particular value for imparting survivaland yield in areas where a particular crop would not normally prosper.

Summary of Altered Drought-Related Plant Characteristics.

The clades of structurally and functionally related sequences thatderive from a wide range of plants, including polynucleotides of theSequence Listing and their encoded polypeptides, fragments thereof,paralogs, orthologs, equivalogs, and fragments thereof, is provided.These sequences have been shown in laboratory and field experiments toconfer altered size and abiotic stress tolerance phenotypes in plants.The invention also provides the polypeptides of the Sequence Listing,and fragments thereof, conserved domains thereof, paralogs, orthologs,equivalogs, and fragments thereof. Plants that overexpress thesesequences have been observed to exhibit a sugar sensing phenotype and/orbe more tolerant to a wide variety of abiotic stresses, includingdrought and high salt stress. Many of the orthologs of these sequencesare listed in the Sequence Listing, and due to the high degree ofstructural similarity to the sequences of the invention, it is expectedthat these sequences will also function to increase drought stresstolerance. The invention also encompasses the complements of thepolynucleotides. The polynucleotides are useful for screening librariesof molecules or compounds for specific binding and for creatingtransgenic plants having increased drought stress tolerance.

Potential Applications of Polynucleotides and Polypeptides that RegulateC/N Sensing.

The genes identified by the experiments detailed in this reportrepresent potential regulators of plant responses to low nutrientconditions. As such, these genes (or their putative orthologs andparalogs) could be applied to commercial species in order to improveyield, improve performance under conditions of nutrient limitation, andsubstantially reduce the necessity for fertilizer application.

The data of Lam et al. (Lam (2003) Plant Physiol. 132: 926-935) suggestthat quantitative changes in seed nitrogen reserves may require enhancedtransportation of nitrogen resources. These data further suggest thatthe C/N sensing screen detailed in the below Examples can provide leadswhich, based on low anthocyanin accumulation, could be used to createtransgenic plants with enhanced seed nitrogen reserves.

The experiments performed with specific sequences and transgenic plants,described in Example IX (below), also identified genes which producedelevated levels of anthocyanin, relative to controls, when lines weretested in the C/N assay. In a number of instances, such an effect wasnot alleviated by the provision of an organic nitrogen source such asglutamine, suggesting that the genes were producing a non-specificincrease in anthocyanin levels. Although such results might not berelated to nutrient limitation they likely reveal genes that haveimportant roles in the production of or accumulation of secondarymetabolites related to the phenylpropanoid pathway. A variety ofapplications can be envisaged for such regulatory genes. Uses includealtering pigment production for horticultural purposes and increasingstress resistance. For example, flavonoids have antimicrobial activityand could be used to engineer pathogen resistance. In addition, severalflavonoid compounds have health promoting effects such as the inhibitionof tumor growth, prevention of bone loss and the prevention of theoxidation of lipids. Since the phenylpropanoid biosynthetic pathwayfeeds into the pathways for the production of a number of other classesof secondary metabolites, such as lignins and tannins, changing theactivity of these genes or their paralogs/orthologs might also influencethe levels of those types of compounds. For example, increased levels ofcondensed tannins in forage legumes can prevent pasture bloat in cattleby collapsing protein foams within the rumen. Additionally, lignins areof major interest to the forestry and pulp and paper industries.Elevated levels of lignin increase the quality of wood used forfurniture and building materials. However, paper manufacturers desirereduced lignin levels, since these compounds are costly to remove duringthe pulping process.

Both light and the C/N metabolic status of the plant tightly regulatethe uptake, assimilation, and transport of nitrogen from sources (e.g.leaves) to sinks (e.g. developing seeds). We used an assay that has beendeveloped to detect alterations in the mechanisms that plants use tosense internal levels of carbon and nitrogen metabolites and presumablyactivate signal transduction cascades which regulate the transcriptionof N-assimilatory genes (Hsieh et al. (1998) Proc. Natl. Acad. Sci. 95:13965-13970). To determine whether the mechanisms used to sense nitrogenstatus are altered in a particular mutant or transgenic line, weexploited the observation that seedlings of wild-type plants accumulatehigh levels of anthocyanins when the C/N balance is disturbed. This wasachieved by germinating these plants on media containing high levels ofsucrose (3%) without a nitrogen source. Sucrose-induced anthocyaninaccumulation may be relieved by the addition of either inorganic ororganic nitrogen. Thus, media containing glutamine as a nitrogen sourcewas also used in C/N sensing assays since glutamine also serves as acompound used to transport N in plants.

The clades of sequences shown in laboratory experiments to conferaltered C/N sensing in plants, and structurally and functionally relatedsequences that derive from a wide range of plants, including thepolynucleotides and polypeptides of the invention (for example, SEQ IDNO: 234, 286, 312, 324, 420, 422, 424, 294, 426, 428, 430, 432, 434,436, 438, 240, 440, 442, 444, 446, 448, 450, 452, 454, 456, 458, 460,462, 248, 464, 466, 468, 470, 472, 474, 476, 478, 480, 482, 484, 486,488, 490, 492, 494, 496, 498, 500, 502, 504, 506, 508, 510, 512, 514,516, 518, 520, 522, 238, 524, 526, 528, 530, 532, 534, 536, 538, 540,542, 544, 546, 548, 550, 10, 552, 12, 554, 556, 558, 560, 562, 564, 566,and 568), polypeptides that are encoded by the polynucleotides of theinvention, functional fragments thereof, paralogs, orthologs,equivalogs, and conserved domains thereof are provided. Many of theorthologs of these sequences are listed in the Sequence Listing, and dueto the high degree of structural similarity to the sequences of theinvention, it is expected that these sequences may also function tomodify C/N sensing. The invention also encompasses the complements ofthe polynucleotides. The polynucleotides are useful for screeninglibraries of molecules or compounds for specific binding and forcreating transgenic plants having altered C/N sensing.

Potential Applications of the Presently Disclosed Sequences thatRegulate Shade Tolerance.

The genes identified by the experiment presently disclosed representpotential regulators of plant responses to shade conditions. As such,these genes (or their orthologs and paralogs) could be applied tocommercial species in order to improve yield, and potentially allowcertain crops to be grown at higher density.

While a shade avoidance phenotype has obvious advantages for plantscompeting to survive in the wild, in a crop of identical plants to beharvested at the end of the season, it can be a waste of energy anddetract resources from storage organs, the accumulation of biomass, andthe production of fruits and seeds. Importantly, many plant speciesinitiate a response to shade, due to reflected far-red light fromneighbors, well before light availability becomes a growth-limitingfactor. These effects have a negative impact on yield, and result inincreased volumes of waste by-products, such as straw. In order tocompensate for the inefficiencies produced by shading responses,increased fertilizer applications are required to maintain yield. Thus,genes that suppress innate plant shading responses will offer theadditional advantages of permitting a reduction in fertilizer usage anda reduction in undesirable waste products.

It should be noted that the transcription factor leads revealed in thisstudy likely represent key components of light response pathways and assuch might be used to manipulate additional aspects of plant developmentand physiology. For example, light response regulators might be appliedto manipulate the timing of major growth transitions like the onset offlowering. It should also be recognized that a number of the genesidentified, result in generally compact plant morphologies, and as suchcould be used to produce dwarf varieties that might be attractive forboth grain crops or for ornamental species.

Antisense and Co-Suppression

In addition to expression of the nucleic acids of the invention as genereplacement or plant phenotype modification nucleic acids, the nucleicacids are also useful for sense and anti-sense suppression ofexpression, for example, to down-regulate expression of a nucleic acidof the invention. That is, the nucleic acids of the invention, orsubsequences or anti-sense sequences thereof, can be used to blockexpression of naturally occurring homologous nucleic acids. A variety ofsense and anti-sense technologies are known in the art, for example, asset forth in Lichtenstein and Nellen (1997) Antisense Technology: APractical Approach, IRL Press at Oxford University Press, Oxford, U.K.Antisense regulation is also described in Crowley et al. (1985) Cell 43:633-641; Rosenberg et al. (1985) Nature 313: 703-706; Preiss et al.(1985) Nature 313: 27-32; Melton (1985) Proc. Natl. Acad. Sci. 82:144-148; Izant and Weintraub (1985) Science 229: 345-352; and Kim andWold (1985) Cell 42: 129-138. Additional methods for antisenseregulation are known in the art. Antisense regulation has been used toreduce or inhibit expression of plant genes in, for example in EuropeanPatent Publication No. 271988. Antisense RNA may be used to reduce geneexpression to produce a visible or biochemical phenotypic change in aplant (Smith et al. (1988) Nature, 334: 724-726; Smith et al. (1990)Plant Mol. Biol. 14: 369-379). In general, sense or anti-sense sequencesare introduced into a cell, where they are optionally amplified, forexample, by transcription. Such sequences include both simpleoligonucleotide sequences and catalytic sequences such as ribozymes.

For example, a reduction or elimination of expression (i.e., a“knock-out”) of a transcription factor or transcription factor homologpolypeptide in a transgenic plant, for example, to modify a plant trait,can be obtained by introducing an antisense construct corresponding tothe polypeptide of interest as a cDNA. For antisense suppression, thetranscription factor or homolog cDNA is arranged in reverse orientation(with respect to the coding sequence) relative to the promoter sequencein the expression vector. The introduced sequence need not be the fulllength cDNA or gene, and need not be identical to the cDNA or gene foundin the plant type to be transformed. Typically, the antisense sequenceneed only be capable of hybridizing to the target gene or RNA ofinterest. Thus, where the introduced sequence is of shorter length, ahigher degree of homology to the endogenous transcription factorsequence will be needed for effective antisense suppression. Whileantisense sequences of various lengths can be utilized, preferably, theintroduced antisense sequence in the vector will be at least 30nucleotides in length, and improved antisense suppression will typicallybe observed as the length of the antisense sequence increases.Preferably, the length of the antisense sequence in the vector will begreater than 100 nucleotides. Transcription of an antisense construct asdescribed results in the production of RNA molecules that are thereverse complement of mRNA molecules transcribed from the endogenoustranscription factor gene in the plant cell.

Suppression of endogenous transcription factor gene expression can alsobe achieved using RNA interference, or RNAi. RNAi is apost-transcriptional, targeted gene-silencing technique that usesdouble-stranded RNA (dsRNA) to incite degradation of messenger RNA(mRNA) containing the same sequence as the dsRNA (Constans, (2002) TheScientist 16:36). Small interfering RNAs, or siRNAs are produced in atleast two steps: an endogenous ribonuclease cleaves longer dsRNA intoshorter, 21-23 nucleotide-long RNAs. The siRNA segments then mediate thedegradation of the target mRNA (Zamore, (2001) Nature Struct. Biol.,8:746-50). RNAi has been used for gene function determination in amanner similar to antisense oligonucleotides (Constans, (2002) TheScientist 16:36). Expression vectors that continually express siRNAs intransiently and stably transfected cells have been engineered to expresssmall hairpin RNAs (shRNAs), which get processed in vivo intosiRNAs-like molecules capable of carrying out gene-specific silencing(Brummelkamp et al., (2002) Science 296:550-553, and Paddison, et al.(2002) Genes & Dev. 16:948-958). Post-transcriptional gene silencing bydouble-stranded RNA is discussed in further detail by Hammond et al.(2001) Nature Rev Gen 2: 110-119, Fire et al. (1998) Nature 391: 806-811and Timmons and Fire (1998) Nature 395: 854. Vectors in which RNAencoded by a transcription factor or transcription factor homolog cDNAis over-expressed can also be used to obtain co-suppression of acorresponding endogenous gene, for example, in the manner described inU.S. Pat. No. 5,231,020 by Jorgensen. Such co-suppression (also termedsense suppression) does not require that the entire transcription factorcDNA be introduced into the plant cells, nor does it require that theintroduced sequence be exactly identical to the endogenous transcriptionfactor gene of interest. However, as with antisense suppression, thesuppressive efficiency will be enhanced as specificity of hybridizationis increased, for example, as the introduced sequence is lengthened,and/or as the sequence similarity between the introduced sequence andthe endogenous transcription factor gene is increased.

Vectors expressing an untranslatable form of the transcription factormRNA (for example, sequences comprising one or more stop codon ornonsense mutation) can also be used to suppress expression of anendogenous transcription factor, thereby reducing or eliminating itsactivity and modifying one or more traits. Methods for producing suchconstructs are described in U.S. Pat. No. 5,583,021. Preferably, suchconstructs are made by introducing a premature stop codon into thetranscription factor gene. Alternatively, a plant trait can be modifiedby gene silencing using double-strand RNA (Sharp (1999) Genes andDevelopment 13: 139-141). Another method for abolishing the expressionof a gene is by insertion mutagenesis using the T-DNA of Agrobacteriumtumefaciens. After generating the insertion mutants, the mutants can bescreened to identify those containing the insertion in a transcriptionfactor or transcription factor homolog gene. Plants containing a singletransgene insertion event at the desired gene can be crossed to generatehomozygous plants for the mutation. Such methods are well known to thoseof skill in the art (for example, in Koncz et al. (1992) Methods inArabidopsis Research, World Scientific Publishing Co. Pte. Ltd., RiverEdge, N.J.).

Alternatively, a plant phenotype can be altered by eliminating anendogenous gene, such as a transcription factor or transcription factorhomolog, for example, by homologous recombination (Kempin et al. (1997)Nature 389: 802-803).

A plant trait can also be modified by using the Cre-lox system (forexample, as described in U.S. Pat. No. 5,658,772). A plant genome can bemodified to include first and second lox sites that are then contactedwith a Cre recombinase. If the lox sites are in the same orientation,the intervening DNA sequence between the two sites is excised. If thelox sites are in the opposite orientation, the intervening sequence isinverted.

The polynucleotides and polypeptides of this invention can also beexpressed in a plant in the absence of an expression cassette bymanipulating the activity or expression level of the endogenous gene byother means, such as, for example, by ectopically expressing a gene byT-DNA activation tagging (Ichikawa et al. (1997) Nature 390 698-701;Kakimoto et al. (1996) Science 274: 982-985). This method entailstransforming a plant with a gene tag containing multiple transcriptionalenhancers and once the tag has inserted into the genome, expression of aflanking gene coding sequence becomes deregulated. In another example,the transcriptional machinery in a plant can be modified so as toincrease transcription levels of a polynucleotide of the invention (forexample, in PCT Publications WO 96/06166 and WO 98/53057, which describethe modification of the DNA-binding specificity of zinc finger proteinsby changing particular amino acids in the DNA-binding motif).

The transgenic plant can also include the machinery necessary forexpressing or altering the activity of a polypeptide encoded by anendogenous gene, for example, by altering the phosphorylation state ofthe polypeptide to maintain it in an activated state.

Transgenic plants (or plant cells, or plant explants, or plant tissues)incorporating the polynucleotides of the invention and/or expressing thepolypeptides of the invention can be produced by a variety of wellestablished techniques as described above. Following construction of avector, most typically an expression cassette, including apolynucleotide, for example, encoding a transcription factor ortranscription factor homolog, of the invention, standard techniques canbe used to introduce the polynucleotide into a plant, a plant cell, aplant explant or a plant tissue of interest. Optionally, the plant cell,explant or tissue can be regenerated to produce a transgenic plant.

The plant can be any higher plant, including gymnosperms,monocotyledonous and dicotyledonous plants. Suitable protocols areavailable for Leguminosae (alfalfa, soybean, clover, etc.), Umbelliferae(carrot, celery, parsnip), Cruciferae (cabbage, radish, rapeseed,broccoli, etc.), Curcurbitaceae (melons and cucumber), Gramineae (wheat,corn, rice, barley, millet, etc.), Solanaceae (potato, tomato, tobacco,peppers, etc.), and various other crops (for example, in protocolsdescribed in Ammirato et al., eds., (1984) Handbook of Plant CellCulture—Crop Species, Macmillan Publ. Co., New York, N.Y.; Shimamoto etal. (1989) Nature 338: 274-276; Fromm et al. (1990) Bio/Technol. 8:833-839; and Vasil et al. (1990) Bio/Technol. 8: 429-434.

Transformation and regeneration of both monocotyledonous anddicotyledonous plant cells is now routine, and the selection of the mostappropriate transformation technique will be determined by thepractitioner. The choice of method will vary with the type of plant tobe transformed; those skilled in the art will recognize the suitabilityof particular methods for given plant types. Suitable methods caninclude, but are not limited to: electroporation of plant protoplasts;liposome-mediated transformation; polyethylene glycol (PEG) mediatedtransformation; transformation using viruses; micro-injection of plantcells; micro-projectile bombardment of plant cells; vacuum infiltration;and Agrobacterium tumefaciens mediated transformation. Transformationmeans introducing a nucleotide sequence into a plant in a manner tocause stable or transient expression of the sequence.

Successful examples of the modification of plant characteristics bytransformation with cloned sequences which serve to illustrate thecurrent knowledge in this field of technology, and which are hereinincorporated by reference, include: U.S. Pat. Nos. 5,571,706; 5,677,175;5,510,471; 5,750,386; 5,597,945; 5,589,615; 5,750,871; 5,268,526;5,780,708; 5,538,880; 5,773,269; 5,736,369 and 5,610,042.

Following transformation, plants are preferably selected using adominant selectable marker incorporated into the transformation vector.Typically, such a marker will confer antibiotic or herbicide resistanceon the transformed plants, and selection of transformants can beaccomplished by exposing the plants to appropriate concentrations of theantibiotic or herbicide.

After transformed plants are selected and grown to maturity, thoseplants showing a modified trait are identified. The modified trait canbe any of those traits described above. Additionally, to confirm thatthe modified trait is due to changes in expression levels or activity ofthe polypeptide or polynucleotide of the invention can be determined byanalyzing mRNA expression using Northern blots, RT-PCR or microarrays,or protein expression using immunoblots or Western blots or gel shiftassays.

Integrated Systems—Sequence Identity

Additionally, the present invention may be an integrated system,computer or computer readable medium that comprises an instruction setfor determining the identity of one or more sequences in a database. Inaddition, the instruction set can be used to generate or identifysequences that meet any specified criteria. Furthermore, the instructionset may be used to associate or link certain functional benefits, suchimproved characteristics, with one or more identified sequence.

For example, the instruction set can include, for example, a sequencecomparison or other alignment program, for example, an available programsuch as, for example, the Wisconsin Package Version 10.0, such as BLAST,FASTA, PILEUP, FINDPAT FERNS or the like (GCG, Madison, Wis.). Publicsequence databases such as GenBank, EMBL, Swiss-Prot and PIR or privatesequence databases such as PHYTOSEQ sequence database (Incyte Genomics,Palo Alto, Calif.) can be searched.

Alignment of sequences for comparison can be conducted by the localhomology algorithm of Smith and Waterman (1981) Adv. Appl. Math. 2:482-489, by the homology alignment algorithm of Needleman and Wunsch(1970) J. Mol. Biol. 48: 443-453, by the search for similarity method ofPearson and Lipman (1988) Proc. Natl. Acad. Sci. 85: 2444-2448, bycomputerized implementations of these algorithms. After alignment,sequence comparisons between two (or more) polynucleotides orpolypeptides are typically performed by comparing sequences of the twosequences over a comparison window to identify and compare local regionsof sequence similarity. The comparison window can be a segment of atleast about 20 contiguous positions, usually about 50 to about 200, moreusually about 100 to about 150 contiguous positions. A description ofthe method is provided in Ausubel et al. supra.

A variety of methods for determining sequence relationships can be used,including manual alignment and computer assisted sequence alignment andanalysis. This later approach is a preferred approach in the presentinvention, due to the increased throughput afforded by computer assistedmethods. As noted above, a variety of computer programs for performingsequence alignment are available, or can be produced by one of skill.

One example algorithm that is suitable for determining percent sequenceidentity and sequence similarity is the BLAST algorithm, which isdescribed in Altschul et al. (1990) J. Mol. Biol. 215: 403-410. Softwarefor performing BLAST analyses is publicly available, for example,through the National Library of Medicine's National Center forBiotechnology Information (ncbi.nlm.nih; world wide web (www) NationalInstitutes of Health US government (gov) website). This algorithminvolves first identifying high scoring sequence pairs (HSPs) byidentifying short words of length W in the query sequence, which eithermatch or satisfy some positive-valued threshold score T when alignedwith a word of the same length in a database sequence. T is referred toas the neighborhood word score threshold (Altschul et al. supra). Theseinitial neighborhood word hits act as seeds for initiating searches tofind longer HSPs containing them. The word hits are then extended inboth directions along each sequence for as far as the cumulativealignment score can be increased. Cumulative scores are calculatedusing, for nucleotide sequences, the parameters M (reward score for apair of matching residues; always >0) and N (penalty score formismatching residues; always <0). For amino acid sequences, a scoringmatrix is used to calculate the cumulative score. Extension of the wordhits in each direction are halted when: the cumulative alignment scorefalls off by the quantity X from its maximum achieved value; thecumulative score goes to zero or below, due to the accumulation of oneor more negative-scoring residue alignments; or the end of eithersequence is reached. The BLAST algorithm parameters W, T, and Xdetermine the sensitivity and speed of the alignment. The BLASTN program(for nucleotide sequences) uses as defaults a wordlength (W) of 11, anexpectation (E) of 10, a cutoff of 100, M=5, N=−4, and a comparison ofboth strands. For amino acid sequences, the BLASTP program uses asdefaults a wordlength (W) of 3, an expectation (E) of 10, and theBLOSUM62 scoring matrix (Henikoff and Henikoff (1992) Proc. Natl. Acad.Sci. 89: 10915-10919). Unless otherwise indicated, “sequence identity”here refers to the % sequence identity generated from a tblastx usingthe NCBI version of the algorithm at the default settings using gappedalignments with the filter “off” (for example, in the NIH NLM NCBIwebsite at ncbi.nlm.nih, supra).

In addition to calculating percent sequence identity, the BLASTalgorithm also performs a statistical analysis of the similarity betweentwo sequences (for example, in Karlin and Altschul (1993) Proc. Natl.Acad. Sci. 90: 5873-5787). One measure of similarity provided by theBLAST algorithm is the smallest sum probability (P(N)), which providesan indication of the probability by which a match between two nucleotideor amino acid sequences would occur by chance. For example, a nucleicacid is considered similar to a reference sequence (and, therefore, inthis context, homologous) if the smallest sum probability in acomparison of the test nucleic acid to the reference nucleic acid isless than about 0.1, or less than about 0.01, and or even less thanabout 0.001. An additional example of a useful sequence alignmentalgorithm is PILEUP. PILEUP creates a multiple sequence alignment from agroup of related sequences using progressive, pairwise alignments. Theprogram can align, for example, up to 300 sequences of a maximum lengthof 5,000 letters.

The integrated system, or computer typically includes a user inputinterface allowing a user to selectively view one or more sequencerecords corresponding to the one or more character strings, as well asan instruction set which aligns the one or more character strings witheach other or with an additional character string to identify one ormore region of sequence similarity. The system may include a link of oneor more character strings with a particular phenotype or gene function.Typically, the system includes a user readable output element thatdisplays an alignment produced by the alignment instruction set.

The methods of this invention can be implemented in a localized ordistributed computing environment. In a distributed environment, themethods may be implemented on a single computer comprising multipleprocessors or on a multiplicity of computers. The computers can belinked, for example, through a common bus, but more preferably thecomputer(s) are nodes on a network. The network can be a generalized ora dedicated local or wide-area network and, in certain preferredembodiments, the computers may be components of an intra-net or aninternet.

Thus, the invention provides methods for identifying a sequence similaror homologous to one or more polynucleotides as noted herein, or one ormore target polypeptides encoded by the polynucleotides, or otherwisenoted herein and may include linking or associating a given plantphenotype or gene function with a sequence. In the methods, a sequencedatabase is provided (locally or across an inter or intra net) and aquery is made against the sequence database using the relevant sequencesherein and associated plant phenotypes or gene functions.

Any sequence herein can be entered into the database, before or afterquerying the database. This provides for both expansion of the databaseand, if done before the querying step, for insertion of controlsequences into the database. The control sequences can be detected bythe query to ensure the general integrity of both the database and thequery. As noted, the query can be performed using a web browser basedinterface. For example, the database can be a centralized publicdatabase such as those noted herein, and the querying can be done from aremote terminal or computer across an internet or intranet.

Any sequence herein can be used to identify a similar, homologous,paralogous, or orthologous sequence in another plant. This providesmeans for identifying endogenous sequences in other plants that may beuseful to alter a trait of progeny plants, which results from crossingtwo plants of different strain. For example, sequences that encode anortholog of any of the sequences herein that naturally occur in a plantwith a desired trait can be identified using the sequences disclosedherein. The plant is then crossed with a second plant of the samespecies but which does not have the desired trait to produce progenywhich can then be used in further crossing experiments to produce thedesired trait in the second plant. Therefore the resulting progeny plantcontains no transgenes; expression of the endogenous sequence may alsobe regulated by treatment with a particular chemical or other means,such as EMR. Some examples of such compounds well known in the artinclude: ethylene; cytokinins; phenolic compounds, which stimulate thetranscription of the genes needed for infection; specificmonosaccharides and acidic environments which potentiate vir geneinduction; acidic polysaccharides which induce one or more chromosomalgenes; and opines; other mechanisms include light or dark treatment (forexample, in Winans (1992) Microbiol. Rev. 56: 12-31; Eyal et al. (1992)Plant Mol. Biol. 19: 589-599; Chrispeels et al. (2000) Plant Mol. Biol.42: 279-290; Piazza et al. (2002) Plant Physiol. 128: 1077-1086).

Table 8 lists sequences within the UniGene database determined to beorthologous to a number of transcription factor sequences of the presentinvention. The column headings include the transcription factors listedby (a) the Clade Identifier SEQ ID NO: (the Reference Arabidopsissequence used to identify each clade); (b) the GID of each CladeIdentifier; (c) the AGI Identifier for each Clade Identifier; (d) theUniGene identifier for each orthologous sequence identified in thisstudy; (e) the species from which the orthologs to the transcriptionfactors are derived; and (f) the smallest sum probability relationshipof the homologous sequence to Arabidopsis Clade Identifier sequence in agiven row, determined by BLAST analysis.

TABLE 8 Orthologs of Representative Arabidopsis Transcription FactorGenes Identified Using BLAST Clade AGI Identifier Clade Identifier for(SEQ ID Identifier Clade NO:) (GID) Identifier UniGene IdentifierSpecies p-Value 223 G175 AT4G26440 Les_S5295446 Lycopersicon esculentum1.00E−174 223 G175 AT4G26440 Os_S121030 Oryza sativa 2.00E−77 223 G175AT4G26440 SGN-UNIGENE-57877 Lycopersicon esculentum 1.00E−75 223 G175AT4G26440 Zm_S11524014 Zea mays 9.00E−50 223 G175 AT4G26440SGN-UNIGENE-52888 Lycopersicon esculentum 7.00E−40 223 G175 AT4G26440SGN-UNIGENE-50193 Lycopersicon esculentum 6.00E−36 223 G175 AT4G26440Os_S50781 Oryza sativa 3.00E−19 255 G184 AT4G22070 SGN-UNIGENE-47543Lycopersicon esculentum 1.00E−104 255 G184 AT4G22070 SGN-UNIGENE-47034Lycopersicon esculentum 1.00E−100 255 G184 AT4G22070 Gma_S6668474Glycine max 2.00E−77 255 G184 AT4G22070 SGN-UNIGENE- Lycopersiconesculentum 2.00E−71 SINGLET-18500 255 G184 AT4G22070 SGN-UNIGENE-Lycopersicon esculentum 5.00E−50 SINGLET-1941 255 G184 AT4G22070SGN-UNIGENE- Lycopersicon esculentum 8.00E−37 SINGLET-20683 255 G184AT4G22070 SGN-UNIGENE-52279 Lycopersicon esculentum 5.00E−24 255 G184AT4G22070 Gma_S4878547 Glycine max 2.00E−12 255 G184 AT4G22070SGN-UNIGENE- Lycopersicon esculentum 2.00E−11 SINGLET-2301 255 G184AT4G22070 Hv_S119532 Hordeum vulgare 2.00E−10 255 G184 AT4G22070Zm_S11388469 Zea mays 2.00E−06 257 G186 AT1G62300 SGN-UNIGENE-47543Lycopersicon esculentum 1.00E−104 257 G186 AT1G62300 SGN-UNIGENE-47034Lycopersicon esculentum 1.00E−100 257 G186 AT1G62300 Gma_S6668474Glycine max 2.00E−77 257 G186 AT1G62300 SGN-UNIGENE- Lycopersiconesculentum 2.00E−71 SINGLET-18500 257 G186 AT1G62300 SGN-UNIGENE-Lycopersicon esculentum 5.00E−50 SINGLET-1941 257 G186 AT1G62300SGN-UNIGENE- Lycopersicon esculentum 8.00E−37 SINGLET-20683 257 G186AT1G62300 SGN-UNIGENE-52279 Lycopersicon esculentum 5.00E−24 257 G186AT1G62300 Gma_S4878547 Glycine max 2.00E−12 257 G186 AT1G62300SGN-UNIGENE- Lycopersicon esculentum 2.00E−11 SINGLET-2301 257 G186AT1G62300 Hv_S119532 Hordeum vulgare 2.00E−10 257 G186 AT1G62300Zm_S11388469 Zea mays 2.00E−06 259 G353 AT5G59820 SGN-UNIGENE-56766Lycopersicon esculentum 6.00E−32 259 G353 AT5G59820 Gma_S4898433 Glycinemax 3.00E−26 259 G353 AT5G59820 Ta_S200273 Triticum aestivum 1.00E−24259 G353 AT5G59820 Os_S109163 Oryza sativa 2.00E−20 259 G353 AT5G59820Gma_S4973977 Glycine max 9.00E−17 259 G353 AT5G59820 Ta_S111267 Triticumaestivum 3.00E−16 259 G353 AT5G59820 Mtr_S5397852 Medicago truncatula2.00E−14 259 G353 AT5G59820 Hv_S207187 Hordeum vulgare 5.00E−10 259 G353AT5G59820 Ta_S296415 Triticum aestivum 1.00E−05 227 G354 AT3G46090SGN-UNIGENE-56766 Lycopersicon esculentum 6.00E−32 227 G354 AT3G46090Gma_S4898433 Glycine max 3.00E−26 227 G354 AT3G46090 Ta_S200273 Triticumaestivum 1.00E−24 227 G354 AT3G46090 Os_S109163 Oryza sativa 2.00E−20227 G354 AT3G46090 Gma_S4973977 Glycine max 9.00E−17 227 G354 AT3G46090Ta_S111267 Triticum aestivum 3.00E−16 227 G354 AT3G46090 Mtr_S5397852Medicago truncatula 2.00E−14 227 G354 AT3G46090 Hv_S207187 Hordeumvulgare 5.00E−10 227 G354 AT3G46090 Ta_S296415 Triticum aestivum1.00E−05 229 G489 AT1G08970 Vvi_S16526885 Vitis vinifera 1.00E−77 229G489 AT1G08970 SGN-UNIGENE-45265 Lycopersicon esculentum 4.00E−75 229G489 AT1G08970 Mtr_S5463839 Medicago truncatula 6.00E−73 229 G489AT1G08970 Les_S5293479 Lycopersicon esculentum 2.00E−69 229 G489AT1G08970 Mtr_S7092400 Medicago truncatula 9.00E−66 229 G489 AT1G08970Pta_S17047341 Pinus taeda 7.00E−48 229 G489 AT1G08970 SGN-UNIGENE-45266Lycopersicon esculentum 2.00E−36 229 G489 AT1G08970 Os_S37232 Oryzasativa 5.00E−09 229 G489 AT1G08970 Vvi_S15374122 Vitis vinifera 2.00E−08263 G596 AT2G45430 Pta_S16786360 Pinus taeda 2.00E−70 263 G596 AT2G45430Gma_S4935598 Glycine max 2.00E−67 263 G596 AT2G45430 Pta_S16788492 Pinustaeda 7.00E−63 263 G596 AT2G45430 Pta_S16802054 Pinus taeda 1.00E−57 263G596 AT2G45430 Pta_S15799222 Pinus taeda 6.00E−43 231 G634 AT1G33240Pta_S17050439 Pinus taeda 3.00E−39 231 G634 AT1G33240 Zm_S11449298 Zeamays 3.00E−35 233 G682 AT4G01060 Vvi_S15356289 Vitis vinifera 2.00E−30233 G682 AT4G01060 Ta_S45274 Triticum aestivum 3.00E−14 233 G682AT4G01060 Vvi_S16820566 Vitis vinifera 3.00E−12 233 G682 AT4G01060Gma_S4901946 Glycine max 0.004 265 G714 AT1G54830 Vvi_S16526885 Vitisvinifera 1.00E−77 265 G714 AT1G54830 SGN-UNIGENE-45265 Lycopersiconesculentum 4.00E−75 265 G714 AT1G54830 Mtr_S5463839 Medicago truncatula6.00E−73 265 G714 AT1G54830 Les_S5293479 Lycopersicon esculentum2.00E−69 265 G714 AT1G54830 Mtr_S7092400 Medicago truncatula 9.00E−66265 G714 AT1G54830 Pta_S17047341 Pinus taeda 7.00E−48 265 G714 AT1G54830SGN-UNIGENE-45266 Lycopersicon esculentum 2.00E−36 265 G714 AT1G54830Os_S37232 Oryza sativa 5.00E−09 267 G877 AT5G56270 Les_S5295446Lycopersicon esculentum 1.00E−174 267 G877 AT5G56270 Os_S121030 Oryzasativa 2.00E−77 267 G877 AT5G56270 SGN-UNIGENE-57877 Lycopersiconesculentum 1.00E−75 267 G877 AT5G56270 Zm_S11524014 Zea mays 9.00E−50267 G877 AT5G56270 SGN-UNIGENE-52888 Lycopersicon esculentum 7.00E−40267 G877 AT5G56270 SGN-UNIGENE-50193 Lycopersicon esculentum 6.00E−36267 G877 AT5G56270 Os_S50781 Oryza sativa 3.00E−19 267 G877 AT5G56270SGN-UNIGENE-56707 Lycopersicon esculentum 7.00E−10 235 G916 AT4G04450SGN-UNIGENE-47543 Lycopersicon esculentum 1.00E−104 235 G916 AT4G04450SGN-UNIGENE-47034 Lycopersicon esculentum 1.00E−100 235 G916 AT4G04450Gma_S6668474 Glycine max 2.00E−77 235 G916 AT4G04450 SGN-UNIGENE-Lycopersicon esculentum 2.00E−71 SINGLET-18500 235 G916 AT4G04450SGN-UNIGENE- Lycopersicon esculentum 5.00E−50 SINGLET-1941 235 G916AT4G04450 SGN-UNIGENE- Lycopersicon esculentum 8.00E−37 SINGLET-20683235 G916 AT4G04450 SGN-UNIGENE-52279 Lycopersicon esculentum 5.00E−24235 G916 AT4G04450 Gma_S4878547 Glycine max 2.00E−12 235 G916 AT4G04450Hv_S119532 Hordeum vulgare 2.00E−10 235 G916 AT4G04450 Zm_S11388469 Zeamays 2.00E−06 237 G975 AT1G15360 SGN-UNIGENE- Lycopersicon esculentum9.00E−59 SINGLET-335836 237 G975 AT1G15360 SGN-UNIGENE- Lycopersiconesculentum 2.00E−52 SINGLET-14957 239 G1069 AT4G14465 SGN-UNIGENE-59076Lycopersicon esculentum 6.00E−55 239 G1069 AT4G14465 Vvi_S16805621 Vitisvinifera 1.00E−04 271 G1387 AT5G25390 SGN-UNIGENE- Lycopersiconesculentum 9.00E−59 SINGLET-335836 271 G1387 AT5G25390 SGN-UNIGENE-Lycopersicon esculentum 2.00E−52 SINGLET-14957 273 G1634 AT5G05790Vvi_S16872328 Vitis vinifera 4.00E−63 273 G1634 AT5G05790 SGN-UNIGENE-Lycopersicon esculentum 5.00E−34 SINGLET-48341 273 G1634 AT5G05790SGN-UNIGENE- Lycopersicon esculentum 4.00E−12 SINGLET-41892 275 G1889AT2G28710 SGN-UNIGENE-56766 Lycopersicon esculentum 6.00E−32 275 G1889AT2G28710 Gma_S4898433 Glycine max 3.00E−26 275 G1889 AT2G28710Ta_S200273 Triticum aestivum 1.00E−24 275 G1889 AT2G28710 Os_S109163Oryza sativa 2.00E−20 275 G1889 AT2G28710 Gma_S4973977 Glycine max9.00E−17 275 G1889 AT2G28710 Ta_S111267 Triticum aestivum 3.00E−16 275G1889 AT2G28710 Mtr_S5397852 Medicago truncatula 2.00E−14 275 G1889AT2G28710 Hv_S207187 Hordeum vulgare 5.00E−10 277 G1940 AT5G54900SGN-UNIGENE-44207 Lycopersicon esculentum 1.00E−144 277 G1940 AT5G54900Zm_S11525357 Zea mays 1.00E−130 277 G1940 AT5G54900 Zm_S11522955 Zeamays 1.00E−100 277 G1940 AT5G54900 Vvi_S16865171 Vitis vinifera 1.00E−85277 G1940 AT5G54900 Hv_S153237 Hordeum vulgare 9.00E−72 277 G1940AT5G54900 Ta_S152820 Triticum aestivum 1.00E−66 277 G1940 AT5G54900SGN-UNIGENE- Lycopersicon esculentum 3.00E−55 SINGLET-396174 277 G1940AT5G54900 SGN-UNIGENE- Lycopersicon esculentum 4.00E−53 SINGLET-333119277 G1940 AT5G54900 Gma_S4975207 Glycine max 6.00E−51 277 G1940AT5G54900 SGN-UNIGENE- Lycopersicon esculentum 1.00E−51 SINGLET-17539277 G1940 AT5G54900 Hv_S63965 Hordeum vulgare 4.00E−43 277 G1940AT5G54900 SGN-UNIGENE-56600 Lycopersicon esculentum 2.00E−43 277 G1940AT5G54900 Os_S32676 Oryza sativa 2.00E−31 277 G1940 AT5G54900 Ta_S125786Triticum aestivum 6.00E−26 277 G1940 AT5G54900 Ta_S267457 Triticumaestivum 5.00E−24 277 G1940 AT5G54900 Vvi_S16866336 Vitis vinifera7.00E−18 277 G1940 AT5G54900 Os_S75860 Oryza sativa 4.00E−11 277 G1940AT5G54900 SGN-UNIGENE- Lycopersicon esculentum 2.00E−04 SINGLET-49629279 G1974 AT3G46070 SGN-UNIGENE-56766 Lycopersicon esculentum 6.00E−32279 G1974 AT3G46070 Gma_S4898433 Glycine max 3.00E−26 279 G1974AT3G46070 Ta_S200273 Triticum aestivum 1.00E−24 279 G1974 AT3G46070Os_S109163 Oryza sativa 2.00E−20 279 G1974 AT3G46070 Gma_S4973977Glycine max 9.00E−17 279 G1974 AT3G46070 Ta_S111267 Triticum aestivum3.00E−16 279 G1974 AT3G46070 Mtr_S5397852 Medicago truncatula 2.00E−14279 G1974 AT3G46070 Hv_S207187 Hordeum vulgare 5.00E−10 279 G1974AT3G46070 Ta_S296415 Triticum aestivum 1.00E−05 281 G2153 AT3G04570SGN-UNIGENE-59076 Lycopersicon esculentum 6.00E−55 281 G2153 AT3G04570Mtr_S5308977 Medicago truncatula 2.00E−31 281 G2153 AT3G04570 Hv_S52928Hordeum vulgare 5 283 G2583 AT5G11190 SGN-UNIGENE- Lycopersiconesculentum 9.00E−59 SINGLET-335836 283 G2583 AT5G11190 SGN-UNIGENE-Lycopersicon esculentum 2.00E−52 SINGLET-14957 245 G2701 AT3G11280Vvi_S16872328 Vitis vinifera 4.00E−63 245 G2701 AT3G11280 SGN-UNIGENE-Lycopersicon esculentum 5.00E−34 SINGLET-48341 245 G2701 AT3G11280SGN-UNIGENE- Lycopersicon esculentum 4.00E−12 SINGLET-41892 247 G2789AT3G60870 Pta_S16786360 Pinus taeda 2.00E−70 247 G2789 AT3G60870Gma_S4935598 Glycine max 2.00E−67 247 G2789 AT3G60870 Pta_S16788492Pinus taeda 7.00E−63 247 G2789 AT3G60870 Pta_S16802054 Pinus taeda1.00E−57 247 G2789 AT3G60870 Pta_S15799222 Pinus taeda 6.00E−43 249G2839 AT3G46080 SGN-UNIGENE-56766 Lycopersicon esculentum 6.00E−32 249G2839 AT3G46080 Gma_S4898433 Glycine max 3.00E−26 249 G2839 AT3G46080Ta_S200273 Triticum aestivum 1.00E−24 249 G2839 AT3G46080 Os_S109163Oryza sativa 2.00E−20 249 G2839 AT3G46080 Gma_S4973977 Glycine max9.00E−17 249 G2839 AT3G46080 Ta_S111267 Triticum aestivum 3.00E−16 249G2839 AT3G46080 Mtr_S5397852 Medicago truncatula 2.00E−14 249 G2839AT3G46080 Hv_S207187 Hordeum vulgare 5.00E−10 249 G2839 AT3G46080Ta_S296415 Triticum aestivum 1.00E−05 251 G2854 AT4G27000SGN-UNIGENE-44207 Lycopersicon esculentum 1.00E−144 251 G2854 AT4G27000Zm_S11525357 Zea mays 1.00E−130 251 G2854 AT4G27000 Zm_S11522955 Zeamays 1.00E−100 251 G2854 AT4G27000 Vvi_S16865171 Vitis vinifera 1.00E−85251 G2854 AT4G27000 Hv_S153237 Hordeum vulgare 9.00E−72 251 G2854AT4G27000 Ta_S152820 Triticum aestivum 1.00E−66 251 G2854 AT4G27000SGN-UNIGENE- Lycopersicon esculentum 3.00E−55 SINGLET-396174 251 G2854AT4G27000 SGN-UNIGENE- Lycopersicon esculentum 4.00E−53 SINGLET-333119251 G2854 AT4G27000 Gma_S4975207 Glycine max 6.00E−51 251 G2854AT4G27000 SGN-UNIGENE- Lycopersicon esculentum 1.00E−51 SINGLET-17539251 G2854 AT4G27000 Hv_S63965 Hordeum vulgare 4.00E−43 251 G2854AT4G27000 SGN-UNIGENE-56600 Lycopersicon esculentum 2.00E−43 251 G2854AT4G27000 Os_S32676 Oryza sativa 2.00E−31 251 G2854 AT4G27000 Ta_S125786Triticum aestivum 6.00E−26 251 G2854 AT4G27000 Ta_S267457 Triticumaestivum 5.00E−24 251 G2854 AT4G27000 Vvi_S16866336 Vitis vinifera7.00E−18 251 G2854 AT4G27000 Os_S75860 Oryza sativa 4.00E−11 251 G2854AT4G27000 SGN-UNIGENE- Lycopersicon esculentum 2.00E−04 SINGLET-49629253 G3083 AT3G14880 Gma_S4880456 Glycine max 1.00E−25 253 G3083AT3G14880 Ta_S179586 Triticum aestivum 1.00E−13 253 G3083 AT3G14880Os_S54214 Oryza sativa 5.00E−08 253 G3083 AT3G14880 Hv_S60182 Hordeumvulgare 3.00E−06 463 G8 AT2G28550 SGN-UNIGENE- Lycopersicon esculentum1.00E−64 SINGLET-395477 463 G8 AT2G28550 Ta_S177690 Triticum aestivum2.00E−21 463 G8 AT2G28550 Vvi_S15411435 Vitis vinifera 6.00E−07 419 G24AT2G23340 Gma_S5071803 Glycine max 8.00E−40 419 G24 AT2G23340SGN-UNIGENE-49683 Lycopersicon esculentum 1.00E−14 419 G24 AT2G23340SGN-UNIGENE-54594 Lycopersicon esculentum 4.00E−41 419 G24 AT2G23340SGN-UNIGENE- Lycopersicon esculentum 7.00E−19 SINGLET-47313 419 G24AT2G23340 Mtr_S5349908 Medicago truncatula 4.00E−32 419 G24 AT2G23340Os_S32369 Oryza sativa 1.00E−13 419 G24 AT2G23340 Os_S80194 Oryza sativa4.00E−08 419 G24 AT2G23340 Vvi_S15370190 Vitis vinifera 1.00E−38 419 G24AT2G23340 Vvi_S16806812 Vitis vinifera 6.00E−25 421 G154 AT2G45660Gma_S5094568 Glycine max 2.00E−13 421 G154 AT2G45660 Les_S5295933Lycopersicon esculentum 2.00E−57 421 G154 AT2G45660 SGN-UNIGENE-50586Lycopersicon esculentum 4.00E−56 421 G154 AT2G45660 SGN-UNIGENE-52410Lycopersicon esculentum 2.00E−54 421 G154 AT2G45660 SGN-UNIGENE-Lycopersicon esculentum 2.00E−27 SINGLET-366830 421 G154 AT2G45660SGN-UNIGENE- Lycopersicon esculentum 3.00E−47 SINGLET-394847 421 G154AT2G45660 Mtr_S5357829 Medicago truncatula 2.00E−53 421 G154 AT2G45660Os_S60918 Oryza sativa 1.00E−57 421 G154 AT2G45660 Pta_S15732813 Pinustaeda 5.00E−13 421 G154 AT2G45660 Pta_S15736271 Pinus taeda 2.00E−37 421G154 AT2G45660 Pta_S15739572 Pinus taeda 4.00E−22 421 G154 AT2G45660Pta_S15740527 Pinus taeda 8.00E−31 421 G154 AT2G45660 Pta_S15746398Pinus taeda 6.00E−26 421 G154 AT2G45660 Pta_S15751737 Pinus taeda2.00E−39 421 G154 AT2G45660 Pta_S15777399 Pinus taeda 3.00E−22 421 G154AT2G45660 Pta_S15780122 Pinus taeda 1.00E−36 421 G154 AT2G45660Pta_S15795745 Pinus taeda 1.00E−23 421 G154 AT2G45660 Pta_S16849782Pinus taeda 3.00E−55 421 G154 AT2G45660 Ta_S203038 Triticum aestivum3.00E−47 421 G154 AT2G45660 Ta_S424724 Triticum aestivum 8.00E−19 421G154 AT2G45660 Vvi_S15373999 Vitis vinifera 4.00E−72 421 G154 AT2G45660Vvi_S16872184 Vitis vinifera 7.00E−35 421 G154 AT2G45660 Zm_S11418746Zea mays 2.00E−58 421 G154 AT2G45660 Zm_S11527819 Zea mays 6.00E−55 467G156 AT5G23260 SGN-UNIGENE-54690 Lycopersicon esculentum 5.00E−40 469G161 AT5G60440 SGN-UNIGENE-57990 Lycopersicon esculentum 3.00E−20 475G189 AT2G23320 Gma_S4901804 Glycine max 3.00E−15 475 G189 AT2G23320Les_S6657758 Lycopersicon esculentum 2.00E−22 475 G189 AT2G23320Pta_S16793418 Pinus taeda 1.00E−36 475 G189 AT2G23320 Vvi_S15353287Vitis vinifera 1.00E−29 475 G189 AT2G23320 Vvi_S15374453 Vitis vinifera9.00E−32 477 G200 AT1G08810 SGN-UNIGENE-57276 Lycopersicon esculentum9.00E−10 477 G200 AT1G08810 SGN-UNIGENE- Lycopersicon esculentum1.00E−61 SINGLET-385670 477 G200 AT1G08810 Os_S60479 Oryza sativa9.00E−71 477 G200 AT1G08810 Zm_S11529138 Zea mays 9.00E−18 477 G200AT1G08810 Zm_S11529143 Zea mays 1.00E−19 477 G200 AT1G08810 Zm_S11529165Zea mays 8.00E−19 479 G234 AT3G49690 SGN-UNIGENE- Lycopersiconesculentum 3.00E−57 SINGLET-21166 479 G234 AT3G49690 Zm_S11529159 Zeamays 3.00E−15 479 G234 AT3G49690 Zm_S11529194 Zea mays 3.00E−16 483 G275AT5G64030 Gma_S4898629 Glycine max 1.00E−93 483 G275 AT5G64030Gma_S4907362 Glycine max 1.00E−16 483 G275 AT5G64030 Hv_S8292 Hordeumvulgare 2.00E−71 483 G275 AT5G64030 SGN-UNIGENE-47489 Lycopersiconesculentum  1.0e−999 483 G275 AT5G64030 SGN-UNIGENE-47510 Lycopersiconesculentum 1.00E−121 483 G275 AT5G64030 SGN-UNIGENE-51256 Lycopersiconesculentum 1.00E−142 483 G275 AT5G64030 SGN-UNIGENE-56050 Lycopersiconesculentum 2.00E−54 483 G275 AT5G64030 Mtr_S10821012 Medicago truncatula1.00E−117 483 G275 AT5G64030 Pta_S15736214 Pinus taeda 1.00E−48 483 G275AT5G64030 Pta_S15776645 Pinus taeda 1.00E−74 483 G275 AT5G64030Vvi_S15426449 Vitis vinifera 1.00E−118 483 G275 AT5G64030 Vvi_S16870363Vitis vinifera 6.00E−23 483 G275 AT5G64030 Zm_S11528144 Zea mays 1.0e−999 485 G326 AT2G33500 Hv_S67575 Hordeum vulgare 4.00E−12 485 G326AT2G33500 SGN-UNIGENE- Lycopersicon esculentum 1.00E−45 SINGLET-19083485 G326 AT2G33500 Pta_S17049915 Pinus taeda 9.00E−17 485 G326 AT2G33500Ta_S148486 Triticum aestivum 2.00E−12 485 G326 AT2G33500 Zm_S11450524Zea mays 1.00E−18 485 G326 AT2G33500 Zm_S11510508 Zea mays 1.00E−11 487G347 AT4G20380 Gma_S4934838 Glycine max 1.00E−12 487 G347 AT4G20380Les_S5275585 Lycopersicon esculentum 3.00E−22 487 G347 AT4G20380SGN-UNIGENE-51747 Lycopersicon esculentum 5.00E−29 487 G347 AT4G20380Mtr_S5454462 Medicago truncatula 1.00E−72 487 G347 AT4G20380 Os_S100515Oryza sativa 9.00E−09 487 G347 AT4G20380 Ta_S64707 Triticum aestivum2.00E−54 487 G347 AT4G20380 Vvi_S16531517 Vitis vinifera 3.00E−66 487G347 AT4G20380 Zm_S11437336 Zea mays 1.00E−19 487 G347 AT4G20380Zm_S11520104 Zea mays 3.00E−53 423 G384 AT4G21750 Gma_S4992142 Glycinemax 3.00E−23 423 G384 AT4G21750 Hv_S30279 Hordeum vulgare 7.00E−22 423G384 AT4G21750 SGN-UNIGENE- Lycopersicon esculentum 4.00E−60SINGLET-17776 423 G384 AT4G21750 Mtr_S5447672 Medicago truncatula1.00E−123 423 G384 AT4G21750 Os_S112966 Oryza sativa  1.0e−999 423 G384AT4G21750 Os_S113503 Oryza sativa 2.00E−93 423 G384 AT4G21750 Ta_S133393Triticum aestivum 3.00E−12 423 G384 AT4G21750 Zm_S11333633 Zea mays1.00E−28 423 G384 AT4G21750 Zm_S11401894 Zea mays 9.00E−16 423 G384AT4G21750 Zm_S11418286 Zea mays  1.0e−999 423 G384 AT4G21750Zm_S11418453 Zea mays  1.0e−999 423 G384 AT4G21750 Zm_S11418455 Zea mays 1.0e−999 423 G384 AT4G21750 Zm_S11523949 Zea mays 4.00E−09 489 G427AT5G11060 Gma_S4867945 Glycine max 7.00E−49 489 G427 AT5G11060 Hv_S23303Hordeum vulgare 3.00E−82 489 G427 AT5G11060 Les_S5295728 Lycopersiconesculentum 1.00E−125 489 G427 AT5G11060 Les_S5295749 Lycopersiconesculentum 1.00E−137 489 G427 AT5G11060 SGN-UNIGENE-51523 Lycopersiconesculentum 2.00E−46 489 G427 AT5G11060 SGN-UNIGENE-54900 Lycopersiconesculentum 5.00E−12 489 G427 AT5G11060 SGN-UNIGENE-55550 Lycopersiconesculentum 1.00E−140 489 G427 AT5G11060 SGN-UNIGENE-55551 Lycopersiconesculentum 4.00E−49 489 G427 AT5G11060 SGN-UNIGENE- Lycopersiconesculentum 4.00E−16 SINGLET-397654 489 G427 AT5G11060 SGN-UNIGENE-Lycopersicon esculentum 8.00E−09 SINGLET-446384 489 G427 AT5G11060SGN-UNIGENE- Lycopersicon esculentum 2.00E−75 SINGLET-50339 489 G427AT5G11060 SGN-UNIGENE- Lycopersicon esculentum 3.00E−49 SINGLET-9520 489G427 AT5G11060 Mtr_S5306926 Medicago truncatula 7.00E−38 489 G427AT5G11060 Mtr_S5449876 Medicago truncatula 2.00E−82 489 G427 AT5G11060Mtr_S7092065 Medicago truncatula 5.00E−85 489 G427 AT5G11060 Os_S60901Oryza sativa 5.00E−89 489 G427 AT5G11060 Os_S64872 Oryza sativa 2.00E−94489 G427 AT5G11060 Os_S64899 Oryza sativa 1.00E−118 489 G427 AT5G11060Os_S64900 Oryza sativa 1.00E−114 489 G427 AT5G11060 Pta_S16847381 Pinustaeda 1.00E−110 489 G427 AT5G11060 Pta_S17051722 Pinus taeda 4.00E−66489 G427 AT5G11060 Ta_S16327 Triticum aestivum 3.00E−93 489 G427AT5G11060 Ta_S201090 Triticum aestivum 2.00E−47 489 G427 AT5G11060Vvi_S15401282 Vitis vinifera 8.00E−19 489 G427 AT5G11060 Vvi_S15423741Vitis vinifera 4.00E−58 489 G427 AT5G11060 Zm_S11442066 Zea mays2.00E−08 489 G427 AT5G11060 Zm_S11452342 Zea mays 3.00E−48 489 G427AT5G11060 Zm_S11527509 Zea mays 4.00E−86 425 G545 AT1G27730 Gma_S4873409Glycine max 1.00E−50 425 G545 AT1G27730 Gma_S5146663 Glycine max2.00E−55 425 G545 AT1G27730 SGN-UNIGENE-44163 Lycopersicon esculentum1.00E−56 425 G545 AT1G27730 SGN-UNIGENE-44287 Lycopersicon esculentum2.00E−35 425 G545 AT1G27730 SGN-UNIGENE- Lycopersicon esculentum4.00E−33 SINGLET-6983 425 G545 AT1G27730 Mtr_S5317695 Medicagotruncatula 4.00E−55 425 G545 AT1G27730 Mtr_S5431156 Medicago truncatula5.00E−40 425 G545 AT1G27730 Ta_S147812 Triticum aestivum 9.00E−16 425G545 AT1G27730 Ta_S66284 Triticum aestivum 5.00E−35 425 G545 AT1G27730Vvi_S15355617 Vitis vinifera 1.00E−52 425 G545 AT1G27730 Vvi_S15382170Vitis vinifera 7.00E−47 425 G545 AT1G27730 Zm_S11441492 Zea mays7.00E−30 425 G545 AT1G27730 Zm_S11443346 Zea mays 1.00E−34 425 G545AT1G27730 Zm_S11465527 Zea mays 2.00E−18 493 G590 AT4G36930SGN-UNIGENE-47483 Lycopersicon esculentum 2.00E−34 493 G590 AT4G36930SGN-UNIGENE-47925 Lycopersicon esculentum 2.00E−41 495 G602 AT2G45820Gma_S4863794 Glycine max 5.00E−55 495 G602 AT2G45820 SGN-UNIGENE-Lycopersicon esculentum 5.00E−04 SINGLET-2565 495 G602 AT2G45820Mtr_S5431439 Medicago truncatula 3.00E−37 495 G602 AT2G45820Pta_S16797626 Pinus taeda 4.00E−46 495 G602 AT2G45820 Vvi_S15353882Vitis vinifera 4.00E−63 495 G602 AT2G45820 Zm_S11527752 Zea mays5.00E−57 497 G618 AT1G53230 Gma_S5029115 Glycine max 9.00E−30 497 G618AT1G53230 Les_S5295478 Lycopersicon esculentum 1.00E−95 497 G618AT1G53230 SGN-UNIGENE-50577 Lycopersicon esculentum 1.00E−52 497 G618AT1G53230 SGN-UNIGENE-58580 Lycopersicon esculentum 1.00E−41 497 G618AT1G53230 SGN-UNIGENE- Lycopersicon esculentum 1.00E−21 SINGLET-24189497 G618 AT1G53230 SGN-UNIGENE- Lycopersicon esculentum 8.00E−30SINGLET-394109 497 G618 AT1G53230 SGN-UNIGENE- Lycopersicon esculentum2.00E−40 SINGLET-401522 497 G618 AT1G53230 Os_S113396 Oryza sativa1.00E−48 497 G618 AT1G53230 Os_S113398 Oryza sativa 1.00E−78 499 G635AT5G63430 Mtr_S5399163 Medicago truncatula 1.00E−40 499 G635 AT5G63430Ta_S2764 Triticum aestivum 6.00E−24 501 G643 AT4G31270 SGN-UNIGENE-56459Lycopersicon esculentum 1.00E−32 503 G653 AT2G39900 Hv_S136844 Hordeumvulgare 1.00E−72 503 G653 AT2G39900 SGN-UNIGENE-46400 Lycopersiconesculentum 4.00E−93 503 G653 AT2G39900 SGN-UNIGENE- Lycopersiconesculentum 2.00E−12 SINGLET-64524 503 G653 AT2G39900 Mtr_S7091176Medicago truncatula 3.00E−51 503 G653 AT2G39900 Os_S76089 Oryza sativa1.00E−37 503 G653 AT2G39900 Pta_S16790444 Pinus taeda 1.00E−40 503 G653AT2G39900 Pta_S17050802 Pinus taeda 2.00E−14 503 G653 AT2G39900Ta_S166473 Triticum aestivum 5.00E−71 503 G653 AT2G39900 Vvi_S15426604Vitis vinifera 2.00E−94 503 G653 AT2G39900 Zm_S11528938 Zea mays7.00E−81 427 G760 AT5G04410 Gma_S4883349 Glycine max 3.00E−09 427 G760AT5G04410 SGN-UNIGENE-47781 Lycopersicon esculentum 1.00E−106 427 G760AT5G04410 SGN-UNIGENE-52634 Lycopersicon esculentum 6.00E−65 427 G760AT5G04410 SGN-UNIGENE-53754 Lycopersicon esculentum 4.00E−72 427 G760AT5G04410 SGN-UNIGENE- Lycopersicon esculentum 5.00E−29 SINGLET-23750427 G760 AT5G04410 SGN-UNIGENE- Lycopersicon esculentum 1.00E−07SINGLET-310313 427 G760 AT5G04410 SGN-UNIGENE- Lycopersicon esculentum3.00E−12 SINGLET-447414 427 G760 AT5G04410 Mtr_S5340844 Medicagotruncatula 6.00E−06 427 G760 AT5G04410 Mtr_S7090764 Medicago truncatula2.00E−14 427 G760 AT5G04410 Pta_S16789085 Pinus taeda 7.00E−36 427 G760AT5G04410 Ta_S202572 Triticum aestivum 5.00E−37 427 G760 AT5G04410Vvi_S16873427 Vitis vinifera 4.00E−21 427 G760 AT5G04410 Zm_S11526816Zea mays 1.00E−16 427 G760 AT5G04410 Zm_S11529038 Zea mays 1.00E−45 429G773 AT3G15500 Gma_S5050636 Glycine max 5.00E−84 429 G773 AT3G15500Les_S5295623 Lycopersicon esculentum 1.00E−105 429 G773 AT3G15500SGN-UNIGENE-45948 Lycopersicon esculentum 1.00E−105 429 G773 AT3G15500SGN-UNIGENE-48215 Lycopersicon esculentum 1.00E−105 507 G837 AT1G29470Gma_S4898629 Glycine max 1.00E−93 507 G837 AT1G29470 Gma_S4907362Glycine max 1.00E−16 507 G837 AT1G29470 Hv_S8292 Hordeum vulgare2.00E−71 507 G837 AT1G29470 SGN-UNIGENE-47489 Lycopersicon esculentum 1.0e−999 507 G837 AT1G29470 SGN-UNIGENE-47510 Lycopersicon esculentum1.00E−121 507 G837 AT1G29470 SGN-UNIGENE-51256 Lycopersicon esculentum1.00E−142 507 G837 AT1G29470 SGN-UNIGENE-56050 Lycopersicon esculentum2.00E−54 507 G837 AT1G29470 Mtr_S10821012 Medicago truncatula 1.00E−117507 G837 AT1G29470 Pta_S15736214 Pinus taeda 1.00E−48 507 G837 AT1G29470Pta_S15776645 Pinus taeda 1.00E−74 507 G837 AT1G29470 Vvi_S15426449Vitis vinifera 1.00E−118 507 G837 AT1G29470 Vvi_S16870363 Vitis vinifera6.00E−23 507 G837 AT1G29470 Zm_S11528144 Zea mays  1.0e−999 509 G866AT2G24570 Gma_S4874203 Glycine max 2.00E−47 509 G866 AT2G24570Gma_S4886425 Glycine max 5.00E−19 509 G866 AT2G24570 Gma_S5106568Glycine max 2.00E−53 509 G866 AT2G24570 Les_S6657761 Lycopersiconesculentum 2.00E−19 509 G866 AT2G24570 Les_S6657762 Lycopersiconesculentum 2.00E−16 509 G866 AT2G24570 SGN-UNIGENE-45903 Lycopersiconesculentum 2.00E−86 509 G866 AT2G24570 SGN-UNIGENE- Lycopersiconesculentum 1.00E−26 SINGLET-439904 509 G866 AT2G24570 Mtr_S5305224Medicago truncatula 2.00E−44 509 G866 AT2G24570 Mtr_S7091692 Medicagotruncatula 1.00E−66 509 G866 AT2G24570 Os_S44434 Oryza sativa 8.00E−42509 G866 AT2G24570 Ta_S174179 Triticum aestivum 8.00E−46 509 G866AT2G24570 Ta_S280279 Triticum aestivum 1.00E−27 509 G866 AT2G24570Vvi_S15374416 Vitis vinifera 9.00E−39 509 G866 AT2G24570 Zm_S11523935Zea mays 1.00E−75 511 G872 AT1G74930 SGN-UNIGENE-50296 Lycopersiconesculentum 7.00E−44 511 G872 AT1G74930 Pta_S15754706 Pinus taeda7.00E−25 511 G872 AT1G74930 Pta_S15767728 Pinus taeda 2.00E−29 511 G872AT1G74930 Pta_S15779272 Pinus taeda 2.00E−28 511 G872 AT1G74930Vvi_S16870232 Vitis vinifera 1.00E−15 515 G912 AT5G51990 Hv_S152300Hordeum vulgare 2.00E−46 515 G912 AT5G51990 Hv_S158942 Hordeum vulgare3.00E−33 515 G912 AT5G51990 Hv_S74288 Hordeum vulgare 4.00E−36 515 G912AT5G51990 Hv_S74289 Hordeum vulgare 4.00E−35 515 G912 AT5G51990Les_S5295301 Lycopersicon esculentum 6.00E−61 515 G912 AT5G51990SGN-UNIGENE-46974 Lycopersicon esculentum 4.00E−50 515 G912 AT5G51990SGN-UNIGENE-46975 Lycopersicon esculentum 2.00E−56 515 G912 AT5G51990SGN-UNIGENE-58571 Lycopersicon esculentum 8.00E−47 515 G912 AT5G51990SGN-UNIGENE- Lycopersicon esculentum 3.00E−35 SINGLET-398604 515 G912AT5G51990 Os_S116938 Oryza sativa 1.00E−36 515 G912 AT5G51990 Os_S116940Oryza sativa 9.00E−33 515 G912 AT5G51990 Os_S117813 Oryza sativa3.00E−44 515 G912 AT5G51990 Os_S65912 Oryza sativa 5.00E−25 515 G912AT5G51990 Ta_S47586 Triticum aestivum 2.00E−20 515 G912 AT5G51990Ta_S75229 Triticum aestivum 2.00E−33 515 G912 AT5G51990 Vvi_S15357313Vitis vinifera 7.00E−09 515 G912 AT5G51990 Vvi_S15391707 Vitis vinifera1.00E−41 515 G912 AT5G51990 Zm_S11519368 Zea mays 3.00E−31 517 G932AT3G47600 Les_S5295595 Lycopersicon esculentum 7.00E−82 517 G932AT3G47600 SGN-UNIGENE-52504 Lycopersicon esculentum 7.00E−81 517 G932AT3G47600 SGN-UNIGENE-52540 Lycopersicon esculentum 1.00E−46 517 G932AT3G47600 SGN-UNIGENE-57232 Lycopersicon esculentum 6.00E−68 517 G932AT3G47600 Vvi_S16532074 Vitis vinifera 2.00E−87 517 G932 AT3G47600Zm_S11524655 Zea mays 4.00E−80 517 G932 AT3G47600 Zm_S11529150 Zea mays7.00E−18 517 G932 AT3G47600 Zm_S11529161 Zea mays 8.00E−16 517 G932AT3G47600 Zm_S11529174 Zea mays 3.00E−15 517 G932 AT3G47600 Zm_S11529193Zea mays 9.00E−18 431 G937 AT1G49560 Gma_S5129137 Glycine max 4.00E−20431 G937 AT1G49560 Vvi_S15431951 Vitis vinifera 2.00E−39 431 G937AT1G49560 Vvi_S16805106 Vitis vinifera 1.00E−16 519 G958 AT1G65910Os_S61189 Oryza sativa 3.00E−55 519 G958 AT1G65910 Os_S69951 Oryzasativa 8.00E−10 519 G958 AT1G65910 Pta_S15738910 Pinus taeda 4.00E−10519 G958 AT1G65910 Pta_S15774939 Pinus taeda 2.00E−33 519 G958 AT1G65910Zm_S11437468 Zea mays 4.00E−19 521 G964 AT5G47370 Gma_S5001940 Glycinemax 3.00E−04 521 G964 AT5G47370 Pta_S15797996 Pinus taeda 1.00E−38 237G975 AT1G15360 SGN-UNIGENE- Lycopersicon esculentum 2.00E−52SINGLET-14957 237 G975 AT1G15360 SGN-UNIGENE- Lycopersicon esculentum9.00E−59 SINGLET-335836 523 G979 AT3G54320 SGN-UNIGENE- Lycopersiconesculentum 5.00E−74 SINGLET-517 523 G979 AT3G54320 Zm_S11528772 Zea mays3.00E−77 435 G988 AT1G55580 Les_S5295726 Lycopersicon esculentum1.00E−114 525 G1049 AT3G30530 Gma_S5131758 Glycine max 2.00E−30 525G1049 AT3G30530 SGN-UNIGENE- Lycopersicon esculentum 5.00E−38SINGLET-333614 525 G1049 AT3G30530 Zm_S11445843 Zea mays 1.00E−17 239G1069 AT4G14465 SGN-UNIGENE-59076 Lycopersicon esculentum 6.00E−55 239G1069 AT4G14465 Vvi_S16805621 Vitis vinifera 1.00E−04 439 G1090AT1G33760 SGN-UNIGENE-54402 Lycopersicon esculentum 3.00E−40 529 G1255AT1G25440 SGN-UNIGENE-48698 Lycopersicon esculentum 5.00E−55 529 G1255AT1G25440 SGN-UNIGENE-53476 Lycopersicon esculentum 1.00E−41 529 G1255AT1G25440 SGN-UNIGENE-54828 Lycopersicon esculentum 9.00E−37 529 G1255AT1G25440 Mtr_S5409553 Medicago truncatula 1.00E−17 529 G1255 AT1G25440Ta_S203158 Triticum aestivum 5.00E−19 529 G1255 AT1G25440 Ta_S363550Triticum aestivum 2.00E−21 529 G1255 AT1G25440 Vvi_S15427527 Vitisvinifera 4.00E−24 529 G1255 AT1G25440 Vvi_S15431583 Vitis vinifera1.00E−24 529 G1255 AT1G25440 Zm_S11485770 Zea mays 1.00E−26 531 G1266AT3G23240 Les_S5269007 Lycopersicon esculentum 2.00E−18 531 G1266AT3G23240 Les_S5295266 Lycopersicon esculentum 2.00E−37 531 G1266AT3G23240 Les_S5295755 Lycopersicon esculentum 8.00E−30 531 G1266AT3G23240 Les_S6682822 Lycopersicon esculentum 8.00E−56 531 G1266AT3G23240 SGN-UNIGENE-48067 Lycopersicon esculentum 3.00E−38 531 G1266AT3G23240 SGN-UNIGENE-49923 Lycopersicon esculentum 9.00E−30 531 G1266AT3G23240 SGN-UNIGENE-52630 Lycopersicon esculentum 2.00E−37 531 G1266AT3G23240 SGN-UNIGENE- Lycopersicon esculentum 6.00E−19 SINGLET-38956441 G1322 AT3G01530 Gma_S4904682 Glycine max 1.00E−17 441 G1322AT3G01530 SGN-UNIGENE-58620 Lycopersicon esculentum 7.00E−67 441 G1322AT3G01530 SGN-UNIGENE- Lycopersicon esculentum 4.00E−42 SINGLET-16950441 G1322 AT3G01530 Vvi_S15388842 Vitis vinifera 4.00E−48 441 G1322AT3G01530 Zm_S11529147 Zea mays 9.00E−13 533 G1331 AT4G13480Zm_S11529198 Zea mays 7.00E−18 537 G1494 AT2G43010 Vvi_S16871195 Vitisvinifera 4.00E−46 539 G1535 AT5G46880 SGN-UNIGENE- Lycopersiconesculentum 4.00E−70 SINGLET-13754 539 G1535 AT5G46880 Os_S98061 Oryzasativa 9.00E−11 539 G1535 AT5G46880 Zm_S11418454 Zea mays 1.00E−180 539G1535 AT5G46880 Zm_S11522858 Zea mays 1.00E−155 445 G1666 AT4G09820Pta_S17046663 Pinus taeda 7.00E−21 543 G1750 AT4G27950 Les_S5295754Lycopersicon esculentum 9.00E−38 543 G1750 AT4G27950 SGN-UNIGENE-49801Lycopersicon esculentum 9.00E−19 543 G1750 AT4G27950 SGN-UNIGENE-Lycopersicon esculentum 1.00E−10 SINGLET-2078 543 G1750 AT4G27950SGN-UNIGENE- Lycopersicon esculentum 3.00E−28 SINGLET-446513 547 G1835AT3G54810 Gma_S4889036 Glycine max 2.00E−33 547 G1835 AT3G54810Gma_S4911179 Glycine max 2.00E−11 547 G1835 AT3G54810 SGN-UNIGENE-48476Lycopersicon esculentum 1.00E−54 547 G1835 AT3G54810 SGN-UNIGENE-51325Lycopersicon esculentum 4.00E−25 547 G1835 AT3G54810 Ta_S142289 Triticumaestivum 2.00E−25 547 G1835 AT3G54810 Ta_S266353 Triticum aestivum1.00E−31 547 G1835 AT3G54810 Vvi_S16865934 Vitis vinifera 1.00E−36 451G1868 AT4G37740 SGN-UNIGENE-48848 Lycopersicon esculentum 4.00E−82 451G1868 AT4G37740 SGN-UNIGENE- Lycopersicon esculentum 5.00E−25SINGLET-453383 451 G1868 AT4G37740 Os_S96499 Oryza sativa 7.00E−04 451G1868 AT4G37740 Pta_S16800293 Pinus taeda 2.00E−08 451 G1868 AT4G37740Ta_S178842 Triticum aestivum 3.00E−11 451 G1868 AT4G37740 Zm_S11522646Zea mays 2.00E−14 451 G1868 AT4G37740 Zm_S11522707 Zea mays 9.00E−11 451G1868 AT4G37740 Zm_S11525236 Zea mays 2.00E−21 453 G1888 AT4G39070SGN-UNIGENE-47593 Lycopersicon esculentum 7.00E−60 453 G1888 AT4G39070Mtr_S10820905 Medicago truncatula 2.00E−48 453 G1888 AT4G39070 Os_S60490Oryza sativa 6.00E−45 453 G1888 AT4G39070 Zm_S11432778 Zea mays 3.00E−19549 G1930 AT3G25730 SGN-UNIGENE-47598 Lycopersicon esculentum 3.00E−52549 G1930 AT3G25730 SGN-UNIGENE- Lycopersicon esculentum 5.00E−57SINGLET-393621 549 G1930 AT3G25730 SGN-UNIGENE- Lycopersicon esculentum6.00E−27 SINGLET-44327 549 G1930 AT3G25730 Mtr_S5430627 Medicagotruncatula 1.00E−63 549 G1930 AT3G25730 Os_S75175 Oryza sativa 3.00E−17549 G1930 AT3G25730 Zm_S11506592 Zea mays 1.00E−37 551 G2057 AT3G15030Gma_S5029115 Glycine max 9.00E−30 551 G2057 AT3G15030 Les_S5295478Lycopersicon esculentum 1.00E−95 551 G2057 AT3G15030 SGN-UNIGENE-50577Lycopersicon esculentum 1.00E−52 551 G2057 AT3G15030 SGN-UNIGENE-58580Lycopersicon esculentum 1.00E−41 551 G2057 AT3G15030 SGN-UNIGENE-Lycopersicon esculentum 1.00E−21 SINGLET-24189 551 G2057 AT3G15030SGN-UNIGENE- Lycopersicon esculentum 8.00E−30 SINGLET-394109 551 G2057AT3G15030 SGN-UNIGENE- Lycopersicon esculentum 2.00E−40 SINGLET-401522551 G2057 AT3G15030 Os_S113396 Oryza sativa 1.00E−48 551 G2057 AT3G15030Os_S113398 Oryza sativa 1.00E−78 457 G2131 AT1G79700 SGN-UNIGENE-Lycopersicon esculentum 5.00E−74 SINGLET-517 457 G2131 AT1G79700Zm_S11528772 Zea mays 3.00E−77 553 G2144 AT3G57800 SGN-UNIGENE-51335Lycopersicon esculentum 1.00E−21 553 G2144 AT3G57800 Vvi_S16529913 Vitisvinifera 3.00E−39 555 G2145 AT1G27740 Ta_S174040 Triticum aestivum3.00E−40 559 G2512 AT1G06160 Hv_S20601 Hordeum vulgare 9.00E−15 559G2512 AT1G06160 SGN-UNIGENE- Lycopersicon esculentum 6.00E−24SINGLET-2865 459 G2520 AT1G59640 Gma_S5045510 Glycine max 2.00E−46 459G2520 AT1G59640 Les_S5183164 Lycopersicon esculentum 1.00E−55 459 G2520AT1G59640 Les_S5203454 Lycopersicon esculentum 1.00E−44 459 G2520AT1G59640 SGN-UNIGENE-44928 Lycopersicon esculentum 4.00E−72 459 G2520AT1G59640 Ta_S84222 Triticum aestivum 3.00E−38 459 G2520 AT1G59640Vvi_S15421316 Vitis vinifera 7.00E−07 459 G2520 AT1G59640 Vvi_S16529182Vitis vinifera 6.00E−61 459 G2520 AT1G59640 Zm_S11524369 Zea mays1.00E−40 461 G2522 AT3G61310 Gma_S4864518 Glycine max 5.00E−24 461 G2522AT3G61310 Hv_S36040 Hordeum vulgare 4.00E−35 461 G2522 AT3G61310SGN-UNIGENE-50326 Lycopersicon esculentum 6.00E−40 461 G2522 AT3G61310Pta_S15767209 Pinus taeda 3.00E−17 461 G2522 AT3G61310 Ta_S115031Triticum aestivum 9.00E−09 461 G2522 AT3G61310 Ta_S65435 Triticumaestivum 4.00E−48 461 G2522 AT3G61310 Vvi_S15370801 Vitis vinifera1.00E−55 563 G2535 AT3G61910 Gma_S5137324 Glycine max 4.00E−12 563 G2535AT3G61910 SGN-UNIGENE- Lycopersicon esculentum 1.00E−72 SINGLET-366637567 G2719 AT3G55730 SGN-UNIGENE- Lycopersicon esculentum 5.00E−52SINGLET-357168 567 G2789 AT3G60870 Gma_S4935598 Glycine max 2.00E−67 247G2789 AT3G60870 Pta_S15799222 Pinus taeda 6.00E−43 247 G2789 AT3G60870Pta_S16786360 Pinus taeda 2.00E−70 247 G2789 AT3G60870 Pta_S16788492Pinus taeda 7.00E−63 247 G2789 AT3G60870 Pta_S16802054 Pinus taeda1.00E−57 423 G38 AT5G05410 Gma_S4861946 Glycine max 6.00E−42 423 G38AT5G05410 Hv_S230730 Hordeum vulgare 4.00E−47 423 G38 AT5G05410Hv_S230731 Hordeum vulgare 3.00E−44 423 G38 AT5G05410 Les_S6682824Lycopersicon esculentum 2.00E−52 423 G38 AT5G05410 Os_S116939 Oryzasativa 9.00E−45 423 G38 AT5G05410 Ta_S266443 Triticum aestivum 9.00E−42423 G38 AT5G05410 Zm_S11524426 Zea mays 4.00E−41 827 G44 AT5G61600Vvi_S15378188 Vitis vinifera 1.00E−04 827 G44 AT5G61600 Vvi_S15402707Vitis vinifera 4.00E−42 827 G44 AT5G61600 Vvi_S16082016 Vitis vinifera1.00E−41 829 G230 AT2G23290 Gma_S4873244 Glycine max 8.00E−08 829 G230AT2G23290 Gma_S4897857 Glycine max 2.00E−69 829 G230 AT2G23290SGN-UNIGENE-46140 Lycopersicon esculentum 1.00E−79 829 G230 AT2G23290SGN-UNIGENE-46445 Lycopersicon esculentum 3.00E−71 829 G230 AT2G23290SGN-UNIGENE- Lycopersicon esculentum 3.00E−45 SINGLET-396033 829 G230AT2G23290 Mtr_S5318648 Medicago truncatula 5.00E−67 829 G230 AT2G23290Mtr_S5421663 Medicago truncatula 1.00E−48 829 G230 AT2G23290Mtr_S5454442 Medicago truncatula 4.00E−09 829 G230 AT2G23290Vvi_S15351083 Vitis vinifera 2.00E−15 829 G230 AT2G23290 Vvi_S15373434Vitis vinifera 4.00E−10 479 G234 AT3G49690 SGN-UNIGENE- Lycopersiconesculentum 3.00E−57 SINGLET-21166 479 G234 AT3G49690 Zm_S11529159 Zeamays 3.00E−15 479 G234 AT3G49690 Zm_S11529194 Zea mays 3.00E−16 831 G261AT4G18880 Gma_S5144289 Glycine max 4.00E−34 831 G261 AT4G18880SGN-UNIGENE-51749 Lycopersicon esculentum 9.00E−76 831 G261 AT4G18880SGN-UNIGENE-59194 Lycopersicon esculentum 3.00E−24 831 G261 AT4G18880Mtr_S7091605 Medicago truncatula 2.00E−50 831 G261 AT4G18880 Os_S23803Oryza sativa 8.00E−12 831 G261 AT4G18880 Os_S83230 Oryza sativa 1.00E−66831 G261 AT4G18880 Pta_S15769714 Pinus taeda 2.00E−45 831 G261 AT4G18880Vvi_S15370308 Vitis vinifera 5.00E−21 831 G261 AT4G18880 Vvi_S15413763Vitis vinifera 4.00E−08 831 G261 AT4G18880 Zm_S11521772 Zea mays6.00E−26 839 G388 AT1G79840 SGN-UNIGENE- Lycopersicon esculentum3.00E−36 SINGLET-2889 839 G388 AT1G79840 SGN-UNIGENE- Lycopersiconesculentum 8.00E−24 SINGLET-393604 839 G388 AT1G79840 Vvi_S15431305Vitis vinifera 3.00E−66 841 G435 AT5G53980 SGN-UNIGENE- Lycopersiconesculentum 1.00E−24 SINGLET-385221 845 G468 AT2G46990 Os_S100653 Oryzasativa 6.00E−05 845 G468 AT2G46990 Vvi_S16820866 Vitis vinifera 5.00E−37847 G571 AT5G06839 SGN-UNIGENE- Lycopersicon esculentum 9.00E−49SINGLET-312251 847 G571 AT5G06839 SGN-UNIGENE- Lycopersicon esculentum3.00E−56 SINGLET-39818 231 G634 AT1G33240 Pta_S17050439 Pinus taeda3.00E−39 231 G634 AT1G33240 Zm_S11449298 Zea mays 3.00E−35 849 G652AT2G21060 Gma_S4871214 Glycine max 2.00E−20 849 G652 AT2G21060Gma_S4965905 Glycine max 3.00E−26 849 G652 AT2G21060 Gma_S5135351Glycine max 1.00E−18 849 G652 AT2G21060 Hv_S142991 Hordeum vulgare6.00E−47 849 G652 AT2G21060 Hv_S147464 Hordeum vulgare 1.00E−22 849 G652AT2G21060 Les_S5162139 Lycopersicon esculentum 3.00E−15 849 G652AT2G21060 SGN-UNIGENE-56979 Lycopersicon esculentum 1.00E−40 849 G652AT2G21060 Os_S46064 Oryza sativa 4.00E−36 849 G652 AT2G21060Pta_S15741898 Pinus taeda 7.00E−49 849 G652 AT2G21060 Ta_S2509 Triticumaestivum 5.00E−05 849 G652 AT2G21060 Ta_S45732 Triticum aestivum1.00E−22 849 G652 AT2G21060 Ta_S60357 Triticum aestivum 6.00E−14 849G652 AT2G21060 Ta_S75244 Triticum aestivum 3.00E−66 849 G652 AT2G21060Vvi_S16864906 Vitis vinifera 5.00E−16 849 G652 AT2G21060 Vvi_S16965349Vitis vinifera 1.00E−18 849 G652 AT2G21060 Zm_S11487070 Zea mays1.00E−51 851 G664 AT4G38620 Gma_S4875209 Glycine max 6.00E−71 851 G664AT4G38620 Gma_S5069370 Glycine max 3.00E−78 851 G664 AT4G38620 Hv_S73887Hordeum vulgare 3.00E−77 851 G664 AT4G38620 Hv_S73888 Hordeum vulgare3.00E−71 851 G664 AT4G38620 Les_S5295913 Lycopersicon esculentum1.00E−89 851 G664 AT4G38620 SGN-UNIGENE-48139 Lycopersicon esculentum1.00E−89 851 G664 AT4G38620 SGN-UNIGENE-52314 Lycopersicon esculentum3.00E−76 851 G664 AT4G38620 SGN-UNIGENE-58669 Lycopersicon esculentum5.00E−49 851 G664 AT4G38620 SGN-UNIGENE- Lycopersicon esculentum3.00E−04 SINGLET-56292 851 G664 AT4G38620 Mtr_S5321074 Medicagotruncatula 2.00E−76 851 G664 AT4G38620 Mtr_S5436024 Medicago truncatula1.00E−38 851 G664 AT4G38620 Os_S60586 Oryza sativa 7.00E−67 851 G664AT4G38620 Os_S96599 Oryza sativa 4.00E−06 851 G664 AT4G38620Pta_S15736913 Pinus taeda 7.00E−65 851 G664 AT4G38620 Pta_S16787963Pinus taeda 3.00E−74 851 G664 AT4G38620 Pta_S16796777 Pinus taeda7.00E−16 851 G664 AT4G38620 Pta_S16796852 Pinus taeda 4.00E−52 851 G664AT4G38620 Pta_S16800437 Pinus taeda 1.00E−21 851 G664 AT4G38620Pta_S16802819 Pinus taeda 2.00E−66 851 G664 AT4G38620 Pta_S17046107Pinus taeda 1.00E−64 851 G664 AT4G38620 Pta_S17052332 Pinus taeda6.00E−29 851 G664 AT4G38620 Ta_S207746 Triticum aestivum 2.00E−73 851G664 AT4G38620 Vvi_S15352484 Vitis vinifera 1.00E−10 851 G664 AT4G38620Vvi_S15427762 Vitis vinifera 3.00E−88 851 G664 AT4G38620 Zm_S11519370Zea mays 2.00E−46 851 G664 AT4G38620 Zm_S11521958 Zea mays 1.00E−73 851G664 AT4G38620 Zm_S11524344 Zea mays 1.00E−79 851 G664 AT4G38620Zm_S11529167 Zea mays 2.00E−18 851 G664 AT4G38620 Zm_S11529181 Zea mays5.00E−18 853 G772 AT3G10480 Gma_S5023840 Glycine max 1.00E−25 853 G772AT3G10480 SGN-UNIGENE-49809 Lycopersicon esculentum 2.00E−87 853 G772AT3G10480 Mtr_S5395615 Medicago truncatula 4.00E−10 855 G798 AT3G50410Mtr_S5415694 Medicago truncatula 2.00E−15 859 G974 AT1G22190Gma_S4897318 Glycine max 3.00E−18 859 G974 AT1G22190 Gma_S4897472Glycine max 3.00E−30 859 G974 AT1G22190 Gma_S4898590 Glycine max2.00E−57 859 G974 AT1G22190 Hv_S10412 Hordeum vulgare 2.00E−08 859 G974AT1G22190 Hv_S70023 Hordeum vulgare 1.00E−14 859 G974 AT1G22190Les_S5182292 Lycopersicon esculentum 4.00E−60 859 G974 AT1G22190SGN-UNIGENE-44095 Lycopersicon esculentum 4.00E−76 859 G974 AT1G22190SGN-UNIGENE-44231 Lycopersicon esculentum 1.00E−68 859 G974 AT1G22190Mtr_S7093809 Medicago truncatula 4.00E−28 859 G974 AT1G22190 Os_S37084Oryza sativa 2.00E−05 859 G974 AT1G22190 Pta_S16845578 Pinus taeda3.00E−26 859 G974 AT1G22190 Ta_S120947 Triticum aestivum 5.00E−11 859G974 AT1G22190 Ta_S184473 Triticum aestivum 1.00E−17 859 G974 AT1G22190Ta_S278378 Triticum aestivum 1.00E−09 859 G974 AT1G22190 Vvi_S15351270Vitis vinifera 3.00E−39 859 G974 AT1G22190 Vvi_S15407610 Vitis vinifera1.00E−60 859 G974 AT1G22190 Zm_S11323940 Zea mays 2.00E−29 859 G974AT1G22190 Zm_S11490783 Zea mays 2.00E−45 859 G974 AT1G22190 Zm_S11528582Zea mays 1.00E−44 435 G988 AT1G55580 Les_S5295726 Lycopersiconesculentum 1.00E−114 807 G1048 AT1G42990 Gma_S4871472 Glycine max3.00E−07 807 G1048 AT1G42990 SGN-UNIGENE-45931 Lycopersicon esculentum2.00E−38 807 G1048 AT1G42990 Mtr_S5316975 Medicago truncatula 7.00E−29807 G1048 AT1G42990 Ta_S244122 Triticum aestivum 3.00E−18 807 G1048AT1G42990 Vvi_S15353884 Vitis vinifera 4.00E−30 807 G1048 AT1G42990Zm_S11527760 Zea mays 1.00E−24 861 G1062 AT3G26744 Gma_S4932282 Glycinemax 5.00E−43 861 G1062 AT3G26744 Les_S5250575 Lycopersicon esculentum5.00E−70 861 G1062 AT3G26744 SGN-UNIGENE-45946 Lycopersicon esculentum1.00E−102 861 G1062 AT3G26744 SGN-UNIGENE- Lycopersicon esculentum5.00E−07 SINGLET-106 861 G1062 AT3G26744 SGN-UNIGENE- Lycopersiconesculentum 2.00E−10 SINGLET-107 861 G1062 AT3G26744 SGN-UNIGENE-Lycopersicon esculentum 2.00E−60 SINGLET-395584 861 G1062 AT3G26744SGN-UNIGENE- Lycopersicon esculentum 1.00E−20 SINGLET-399204 861 G1062AT3G26744 SGN-UNIGENE- Lycopersicon esculentum 2.00E−07 SINGLET-459012861 G1062 AT3G26744 Pta_S15739278 Pinus taeda 4.00E−18 861 G1062AT3G26744 Vvi_S15370409 Vitis vinifera 5.00E−47 239 G1069 AT4G14465SGN-UNIGENE-59076 Lycopersicon esculentum 6.00E−55 239 G1069 AT4G14465Mtr_S5308977 Medicago truncatula 2.00E−31 239 G1069 AT4G14465Vvi_S16805621 Vitis vinifera 1.00E−04 863 G1129 AT4G34530 Vvi_S16532165Vitis vinifera 4.00E−53 865 G1137 AT5G64340 SGN-UNIGENE-48745Lycopersicon esculentum 3.00E−11 865 G1137 AT5G64340 SGN-UNIGENE-48746Lycopersicon esculentum 6.00E−23 657 G1412 AT4G27410 Gma_S5050636Glycine max 5.00E−84 657 G1412 AT4G27410 Les_S5295623 Lycopersiconesculentum 1.00E−105 657 G1412 AT4G27410 SGN-UNIGENE-45948 Lycopersiconesculentum 1.00E−105 657 G1412 AT4G27410 SGN-UNIGENE-48215 Lycopersiconesculentum 1.00E−105 657 G1412 AT4G27410 Vvi_S15352716 Vitis vinifera0.41 867 G1425 AT1G52880 Les_S5247376 Lycopersicon esculentum 6.00E−83867 G1425 AT1G52880 SGN-UNIGENE-44943 Lycopersicon esculentum 1.00E−95867 G1425 AT1G52880 SGN-UNIGENE-46578 Lycopersicon esculentum 8.00E−93867 G1425 AT1G52880 Pta_S16844825 Pinus taeda 1.00E−56 867 G1425AT1G52880 Pta_S17050992 Pinus taeda 2.00E−54 871 G1655 AT1G09250Gma_S4865861 Glycine max 4.00E−17 871 G1655 AT1G09250 SGN-UNIGENE-47983Lycopersicon esculentum 1.00E−37 875 G1789 AT2G21650 Gma_S4886781Glycine max 7.00E−25 875 G1789 AT2G21650 Les_S5295408 Lycopersiconesculentum 2.00E−28 875 G1789 AT2G21650 Ta_S102809 Triticum aestivum3.00E−22 875 G1789 AT2G21650 Ta_S56880 Triticum aestivum 1.00E−18 875G1789 AT2G21650 Vvi_S15406920 Vitis vinifera 3.00E−13 875 G1789AT2G21650 Vvi_S15424752 Vitis vinifera 7.00E−26 875 G1789 AT2G21650Vvi_S16784697 Vitis vinifera 1.00E−27 875 G1789 AT2G21650 Zm_S11328185Zea mays 8.00E−14 875 G1789 AT2G21650 Zm_S11474298 Zea mays 2.00E−16 877G1806 AT1G68640 Gma_S4902665 Glycine max 3.00E−19 877 G1806 AT1G68640Gma_S4911209 Glycine max 5.00E−65 877 G1806 AT1G68640 Gma_S5146796Glycine max 1.00E−139 877 G1806 AT1G68640 Hv_S227616 Hordeum vulgare2.00E−42 877 G1806 AT1G68640 Hv_S27170 Hordeum vulgare 4.00E−52 877G1806 AT1G68640 Les_S5295407 Lycopersicon esculentum 1.00E−120 877 G1806AT1G68640 Les_S5295673 Lycopersicon esculentum 9.00E−99 877 G1806AT1G68640 SGN-UNIGENE-46372 Lycopersicon esculentum 3.00E−78 877 G1806AT1G68640 SGN-UNIGENE-46373 Lycopersicon esculentum 1.00E−134 877 G1806AT1G68640 SGN-UNIGENE-47327 Lycopersicon esculentum 1.00E−139 877 G1806AT1G68640 SGN-UNIGENE-49500 Lycopersicon esculentum 9.00E−51 877 G1806AT1G68640 SGN-UNIGENE-50258 Lycopersicon esculentum 4.00E−89 877 G1806AT1G68640 SGN-UNIGENE-57605 Lycopersicon esculentum 4.00E−06 877 G1806AT1G68640 SGN-UNIGENE-57705 Lycopersicon esculentum 3.00E−84 877 G1806AT1G68640 SGN-UNIGENE-58538 Lycopersicon esculentum 6.00E−97 877 G1806AT1G68640 SGN-UNIGENE- Lycopersicon esculentum 6.00E−04 SINGLET-318510877 G1806 AT1G68640 SGN-UNIGENE- Lycopersicon esculentum 6.00E−26SINGLET-340722 877 G1806 AT1G68640 SGN-UNIGENE- Lycopersicon esculentum8.00E−63 SINGLET-43282 877 G1806 AT1G68640 Mtr_S7091737 Medicagotruncatula 8.00E−29 877 G1806 AT1G68640 Os_S107700 Oryza sativa 4.00E−04877 G1806 AT1G68640 Os_S83289 Oryza sativa 1.00E−144 877 G1806 AT1G68640Os_S83290 Oryza sativa 1.00E−139 877 G1806 AT1G68640 Os_S83291 Oryzasativa 1.00E−139 877 G1806 AT1G68640 Os_S83292 Oryza sativa 1.00E−138877 G1806 AT1G68640 Pta_S17047774 Pinus taeda 1.00E−56 877 G1806AT1G68640 Pta_S17049082 Pinus taeda 5.00E−17 877 G1806 AT1G68640Ta_S115084 Triticum aestivum 1.00E−19 877 G1806 AT1G68640 Ta_S141705Triticum aestivum 5.00E−10 877 G1806 AT1G68640 Ta_S142610 Triticumaestivum 2.00E−15 877 G1806 AT1G68640 Ta_S66308 Triticum aestivum1.00E−136 877 G1806 AT1G68640 Ta_S66461 Triticum aestivum 1.00E−142 877G1806 AT1G68640 Vvi_S15429865 Vitis vinifera 2.00E−76 877 G1806AT1G68640 Vvi_S16526894 Vitis vinifera 1.00E−80 877 G1806 AT1G68640Zm_S11418176 Zea mays 1.00E−141 877 G1806 AT1G68640 Zm_S11418177 Zeamays 1.00E−138 877 G1806 AT1G68640 Zm_S11418513 Zea mays 1.00E−118 877G1806 AT1G68640 Zm_S11425511 Zea mays 6.00E−58 877 G1806 AT1G68640Zm_S11432162 Zea mays 4.00E−29 879 G1911 AT4G39250 Gma_S4886781 Glycinemax 7.00E−25 879 G1911 AT4G39250 Les_S5295408 Lycopersicon esculentum2.00E−28 879 G1911 AT4G39250 Ta_S102809 Triticum aestivum 3.00E−22 879G1911 AT4G39250 Ta_S56880 Triticum aestivum 1.00E−18 879 G1911 AT4G39250Vvi_S15406920 Vitis vinifera 3.00E−13 879 G1911 AT4G39250 Vvi_S15424752Vitis vinifera 7.00E−26 879 G1911 AT4G39250 Vvi_S16784697 Vitis vinifera1.00E−27 879 G1911 AT4G39250 Zm_S11328185 Zea mays 8.00E−14 879 G1911AT4G39250 Zm_S11474298 Zea mays 2.00E−16 813 G1995 AT3G58070SGN-UNIGENE-54039 Lycopersicon esculentum 1.00E−22 813 G1995 AT3G58070SGN-UNIGENE-54252 Lycopersicon esculentum 8.00E−32 813 G1995 AT3G58070SGN-UNIGENE- Lycopersicon esculentum 7.00E−36 SINGLET-392715 813 G1995AT3G58070 Pta_S15742384 Pinus taeda 1.00E−09 881 G2011 AT5G03720Les_S5182191 Lycopersicon esculentum 8.00E−29 881 G2011 AT5G03720SGN-UNIGENE-47254 Lycopersicon esculentum 1.00E−28 881 G2011 AT5G03720Os_S100853 Oryza sativa 1.00E−56 881 G2011 AT5G03720 Ta_S147235 Triticumaestivum 4.00E−14 315 G2155 AT1G14490 Gma_S5081748 Glycine max 2.00E−48315 G2155 AT1G14490 SGN-UNIGENE-48878 Lycopersicon esculentum 5.00E−81315 G2155 AT1G14490 SGN-UNIGENE- Lycopersicon esculentum 8.00E−48SINGLET-471786 315 G2155 AT1G14490 Pta_S16802278 Pinus taeda 2.00E−34885 G2452 AT5G01200 Zm_S11467963 Zea mays 4.00E−15 815 G2467 AT3G63350SGN-UNIGENE-45592 Lycopersicon esculentum 7.00E−57 889 G2510 AT1G01250Gma_S4877810 Glycine max 4.00E−41 889 G2510 AT1G01250 Gma_S5065417Glycine max 2.00E−15 889 G2510 AT1G01250 Mtr_S5455425 Medicagotruncatula 1.00E−49 889 G2510 AT1G01250 Pta_S15772552 Pinus taeda6.00E−29 889 G2510 AT1G01250 Pta_S15778451 Pinus taeda 6.00E−21 889G2510 AT1G01250 Vvi_S15351722 Vitis vinifera 2.00E−27 819 G2550AT1G75410 Mtr_S7094331 Medicago truncatula 8.00E−41 819 G2550 AT1G75410Zm_S11465618 Zea mays 1.00E−47 893 G2571 AT1G64380 SGN-UNIGENE-56732Lycopersicon esculentum 0.25 821 G2640 AT3G51060 SGN-UNIGENE-58699Lycopersicon esculentum 8.00E−42 821 G2640 AT3G51060 SGN-UNIGENE-Lycopersicon esculentum 9.00E−36 SINGLET-461966 895 G2702 AT3G08500Gma_S5127272 Glycine max 2.00E−05 895 G2702 AT3G08500 Pta_S16807545Pinus taeda 3.00E−56 897 G2763 AT3G17100 Pta_S16793632 Pinus taeda2.00E−10 897 G2763 AT3G17100 Vvi_S16806536 Vitis vinifera 6.00E−26 899G2774 AT4G05170 Mtr_S5310210 Medicago truncatula 9.00E−13 247 G2789AT3G60870 Gma_S4935598 Glycine max 2.00E−67 247 G2789 AT3G60870Pta_S15799222 Pinus taeda 6.00E−43 247 G2789 AT3G60870 Pta_S16786360Pinus taeda 2.00E−70 247 G2789 AT3G60870 Pta_S16788492 Pinus taeda7.00E−63 247 G2789 AT3G60870 Pta_S16802054 Pinus taeda 1.00E−57 901G2888 AT1G25250 SGN-UNIGENE- Lycopersicon esculentum 3.00E−37SINGLET-25079 901 G2888 AT1G25250 Os_S101092 Oryza sativa 4.00E−10 901G2888 AT1G25250 Zm_S11429840 Zea mays 2.00E−41

Table 9 lists the gene identification number (GID) and homologousrelationships found using analyses according to the Examples for thesequences of the Sequence Listing. Those sequences listed as “referencesequences” were originally determined by experimentation to conferdrought tolerance when their expression was altered. Generally, eachreference sequence was used to identify the clade in which functionallyrelated homologous sequences may be found.

TABLE 9 Homologs and Other Related Genes of Representative ArabidopsisTranscription Factor Genes Identified using BLAST Polynucleotide SEQ(DNA) or Species from Which ID polypeptide Homologous Relationship ofSEQ ID NO: to Other NO: GID No: (PRT) Sequence is Derived Genes 1 G47DNA Arabidopsis thaliana Reference sequence; predicted polypeptidesequence is paralogous to G2133 2 G47 PRT Arabidopsis thaliana Referencesequence; paralogous to G2133 3 G922 DNA Arabidopsis thaliana Referencesequence 4 G922 PRT Arabidopsis thaliana Reference sequence 5 G1274 DNAArabidopsis thaliana Reference sequence 6 G1274 PRT Arabidopsis thalianaReference sequence 7 G1792 DNA Arabidopsis thaliana Reference sequence 8G1792 PRT Arabidopsis thaliana Reference sequence 9 G2053 DNAArabidopsis thaliana Reference sequence 10 G2053 PRT Arabidopsisthaliana Reference sequence 11 G2133 DNA Arabidopsis thaliana Referencesequence; predicted polypeptide sequence is paralogous to G47 12 G2133PRT Arabidopsis thaliana Reference sequence; paralogous to G47 13 G2999DNA Arabidopsis thaliana Reference sequence 14 G2999 PRT Arabidopsisthaliana Reference sequence 15 G3086 DNA Arabidopsis thaliana Referencesequence 16 G3086 PRT Arabidopsis thaliana Reference sequence 17 G30 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG1792 18 G30 PRT Arabidopsis thaliana Paralogous to G1792 19 G515 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG2053 20 G515 PRT Arabidopsis thaliana Paralogous to G2053 21 G516 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG2053 22 G516 PRT Arabidopsis thaliana Paralogous to G2053 23 G517 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG2053 24 G517 PRT Arabidopsis thaliana Paralogous to G2053 25 G592 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG3086 26 G592 PRT Arabidopsis thaliana Paralogous to G3086 27 G1134 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG3086 28 G1134 PRT Arabidopsis thaliana Paralogous to G3086 29 G1275 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG1274 30 G1275 PRT Arabidopsis thaliana Paralogous to G1274 31 G1758 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG1274 32 G1758 PRT Arabidopsis thaliana Paralogous to G1274 33 G1791 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG1792 34 G1791 PRT Arabidopsis thaliana Paralogous to G1792 35 G1795 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG1792 36 G1795 PRT Arabidopsis thaliana Paralogous to G1792 37 G2149 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG3086 38 G2149 PRT Arabidopsis thaliana Paralogous to G3086 39 G2555 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG3086 40 G2555 PRT Arabidopsis thaliana Paralogous to G3086 41 G2766 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG3086 42 G2766 PRT Arabidopsis thaliana Paralogous to G3086 43 G2989 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG2999 44 G2989 PRT Arabidopsis thaliana Paralogous to G2999 45 G2990 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG2999 46 G2990 PRT Arabidopsis thaliana Paralogous to G2999 47 G2991 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG2999 48 G2991 PRT Arabidopsis thaliana Paralogous to G2999 49 G2992 DNAArabidopsis thaliana Reference sequence; predicted polypeptide sequenceis paralogous to G2999 50 G2992 PRT Arabidopsis thaliana Referencesequence; paralogous to G2999 51 G2993 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G2999 52 G2993 PRTArabidopsis thaliana Paralogous to G2999 53 G2994 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2999 54 G2994PRT Arabidopsis thaliana Paralogous to G2999 55 G2995 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2999 56 G2995PRT Arabidopsis thaliana Paralogous to G2999 57 G2996 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2999 58 G2996PRT Arabidopsis thaliana Paralogous to G2999 59 G2997 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2999 60 G2997PRT Arabidopsis thaliana Paralogous to G2999 61 G2998 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2999 62 G2998PRT Arabidopsis thaliana Paralogous to G2999 63 G3000 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2999 64 G3000PRT Arabidopsis thaliana Paralogous to G2999 65 G3001 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2999 66 G3001PRT Arabidopsis thaliana Paralogous to G2999 67 G3002 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2999 68 G3002PRT Arabidopsis thaliana Paralogous to G2999 69 G3380 DNA Oryza sativaPredicted polypeptide sequence is orthologous to G1792 70 G3380 PRTOryza sativa Orthologous to G1792 71 G3381 DNA Oryza sativa Predictedpolypeptide sequence is orthologous to G1792 72 G3381 PRT Oryza sativaOrthologous to G1792 73 G3383 DNA Oryza sativa Predicted polypeptidesequence is orthologous to G1792 74 G3383 PRT Oryza sativa Orthologousto G1792 75 G3515 DNA Oryza sativa Predicted polypeptide sequence isorthologous to G1792 76 G3515 PRT Oryza sativa Orthologous to G1792 77G3516 DNA Zea mays Predicted polypeptide sequence is orthologous toG1792 78 G3516 PRT Zea mays Orthologous to G1792 79 G3517 DNA Zea maysPredicted polypeptide sequence is orthologous to G1792 80 G3517 PRT Zeamays Orthologous to G1792 81 G3518 DNA Glycine max Predicted polypeptidesequence is orthologous to G1792 82 G3518 PRT Glycine max Orthologous toG1792 83 G3519 DNA Glycine max Predicted polypeptide sequence isorthologous to G1792 84 G3519 PRT Glycine max Orthologous to G1792 85G3520 DNA Glycine max Predicted polypeptide sequence is orthologous toG1792 86 G3520 PRT Glycine max Orthologous to G1792 87 G3643 DNA Glycinemax Predicted polypeptide sequence is orthologous to G47 88 G3643 PRTGlycine max Orthologous to G47 89 G3644 DNA Oryza sativa Predictedpolypeptide sequence is orthologous to G47 90 G3644 PRT Oryza sativaOrthologous to G47 91 G3645 DNA Brassica rapa subsp. Predictedpolypeptide sequence is Pekinensis orthologous to G47 92 G3645 PRTBrassica rapa subsp. Orthologous to G47 Pekinensis 93 G3646 DNA Brassicaoleracea Predicted polypeptide sequence is orthologous to G47 94 G3646PRT Brassica oleracea Orthologous to G47 95 G3647 DNA Zinnia elegansPredicted polypeptide sequence is orthologous to G47 96 G3647 PRT Zinniaelegans Orthologous to G47 97 G3649 DNA Oryza sativa Predictedpolypeptide sequence is orthologous to G47 98 G3649 PRT Oryza sativaOrthologous to G47 99 G3651 DNA Oryza sativa Predicted polypeptidesequence is orthologous to G47 100 G3651 PRT Oryza sativa Orthologous toG47 101 G3663 DNA Lotus corniculatus Predicted polypeptide sequence isvar. japonicus orthologous to G2999 102 G3663 PRT Lotus corniculatusOrthologous to G2999 var. japonicus 103 G3668 DNA Flaveria bidentisPredicted polypeptide sequence is orthologous to G2999 104 G3668 PRTFlaveria bidentis Orthologous to G2999 105 G3670 DNA Lotus corniculatusPredicted polypeptide sequence is var. japonicus orthologous to G2999106 G3670 PRT Lotus corniculatus Orthologous to G2999 var. japonicus 107G3671 DNA Oryza sativa Predicted polypeptide sequence is orthologous toG2999 108 G3671 PRT Oryza sativa Orthologous to G2999 109 G3674 DNAOryza sativa Predicted polypeptide sequence is orthologous to G2999 110G3674 PRT Oryza sativa Orthologous to G2999 111 G3675 DNA Brassica napusPredicted polypeptide sequence is orthologous to G2999 112 G3675 PRTBrassica napus Orthologous to G2999 113 G3680 DNA Zea mays Predictedpolypeptide sequence is orthologous to G2999 114 G3680 PRT Zea maysOrthologous to G2999 115 G3683 DNA Oryza sativa Predicted polypeptidesequence is orthologous to G2999 116 G3683 PRT Oryza sativa Orthologousto G2999 117 G3685 DNA Oryza sativa Predicted polypeptide sequence isorthologous to G2999 118 G3685 PRT Oryza sativa Orthologous to G2999 119G3686 DNA Oryza sativa Predicted polypeptide sequence is orthologous toG2999 120 G3686 PRT Oryza sativa Orthologous to G2999 121 G3690 DNAOryza sativa Predicted polypeptide sequence is orthologous to G2999 122G3690 PRT Oryza sativa Orthologous to G2999 123 G3692 DNA Oryza sativaPredicted polypeptide sequence is orthologous to G2999 124 G3692 PRTOryza sativa Orthologous to G2999 125 G3694 DNA Oryza sativa Predictedpolypeptide sequence is orthologous to G2999 126 G3694 PRT Oryza sativaOrthologous to G2999 127 G3695 DNA Oryza sativa Predicted polypeptidesequence is orthologous to G2999 128 G3695 PRT Oryza sativa Orthologousto G2999 129 G3719 DNA Zea mays Predicted polypeptide sequence isorthologous to G1274 130 G3719 PRT Zea mays Orthologous to G1274 131G3720 DNA Zea mays Predicted polypeptide sequence is orthologous toG1274 132 G3720 PRT Zea mays Orthologous to G1274 133 G3721 DNA Oryzasativa Predicted polypeptide sequence is orthologous to G1274 134 G3721PRT Oryza sativa Orthologous to G1274 135 G3722 DNA Zea mays Predictedpolypeptide sequence is orthologous to G1274 136 G3722 PRT Zea maysOrthologous to G1274 137 G3723 DNA Glycine max Predicted polypeptidesequence is orthologous to G1274 138 G3723 PRT Glycine max Orthologousto G1274 139 G3724 DNA Glycine max Predicted polypeptide sequence isorthologous to G1274 140 G3724 PRT Glycine max Orthologous to G1274 141G3725 DNA Oryza sativa Predicted polypeptide sequence is orthologous toG1274 142 G3725 PRT Oryza sativa Orthologous to G1274 143 G3726 DNAOryza sativa Predicted polypeptide sequence is orthologous to G1274 144G3726 PRT Oryza sativa Orthologous to G1274 145 G3727 DNA Zea maysPredicted polypeptide sequence is orthologous to G1274 146 G3727 PRT Zeamays Orthologous to G1274 147 G3728 DNA Zea mays Predicted polypeptidesequence is orthologous to G1274 148 G3728 PRT Zea mays Orthologous toG1274 149 G3729 DNA Oryza sativa Predicted polypeptide sequence isorthologous to G1274 150 G3729 PRT Oryza sativa Orthologous to G1274 151G3730 DNA Oryza sativa Predicted polypeptide sequence is orthologous toG1274 152 G3730 PRT Oryza sativa Orthologous to G1274 153 G3731 DNALycopersicon Predicted polypeptide sequence is esculentum orthologous toG1274 154 G3731 PRT Lycopersicon Orthologous to G1274 esculentum 155G3732 DNA Solanum tuberosum Predicted polypeptide sequence isorthologous to G1274 156 G3732 PRT Solanum tuberosum Orthologous toG1274 157 G3733 DNA Hordeum vulgare Predicted polypeptide sequence isorthologous to G1274 158 G3733 PRT Hordeum vulgare Orthologous to G1274159 G3735 DNA Medicago truncatula Predicted polypeptide sequence isorthologous to G1792 160 G3735 PRT Medicago truncatula Orthologous toG1792 161 G3736 DNA Triticum aestivum Predicted polypeptide sequence isorthologous to G1792 162 G3736 PRT Triticum aestivum Orthologous toG1792 163 G3737 DNA Oryza sativa Predicted polypeptide sequence isorthologous to G1792 164 G3737 PRT Oryza sativa Orthologous to G1792 165G3739 DNA Zea mays Predicted polypeptide sequence is orthologous toG1792 166 G3739 PRT Zea mays Orthologous to G1792 167 G3740 DNA Oryzasativa Predicted polypeptide sequence is orthologous to G3086 168 G3740PRT Oryza sativa Orthologous to G3086 169 G3741 DNA Oryza sativaPredicted polypeptide sequence is orthologous to G3086 170 G3741 PRTOryza sativa Orthologous to G3086 171 G3742 DNA Oryza sativa Predictedpolypeptide sequence is orthologous to G3086 172 G3742 PRT Oryza sativaOrthologous to G3086 173 G3744 DNA Oryza sativa Predicted polypeptidesequence is orthologous to G3086 174 G3744 PRT Oryza sativa Orthologousto G3086 175 G3746 DNA Oryza sativa Predicted polypeptide sequence isorthologous to G3086 176 G3746 PRT Oryza sativa Orthologous to G3086 177G3755 DNA Zea mays Predicted polypeptide sequence is orthologous toG3086 178 G3755 PRT Zea mays Orthologous to G3086 179 G3763 DNA Glycinemax Predicted polypeptide sequence is orthologous to G3086 180 G3763 PRTGlycine max Orthologous to G3086 181 G3764 DNA Glycine max Predictedpolypeptide sequence is orthologous to G3086 182 G3764 PRT Glycine maxOrthologous to G3086 183 G3765 DNA Glycine max Predicted polypeptidesequence is orthologous to G3086 184 G3765 PRT Glycine max Orthologousto G3086 185 G3766 DNA Glycine max Predicted polypeptide sequence isorthologous to G3086 186 G3766 PRT Glycine max Orthologous to G3086 187G3767 DNA Glycine max Predicted polypeptide sequence is orthologous toG3086 188 G3767 PRT Glycine max Orthologous to G3086 189 G3768 DNAGlycine max Predicted polypeptide sequence is orthologous to G3086 190G3768 PRT Glycine max Orthologous to G3086 191 G3769 DNA Glycine maxPredicted polypeptide sequence is orthologous to G3086 192 G3769 PRTGlycine max Orthologous to G3086 193 G3771 DNA Glycine max Predictedpolypeptide sequence is orthologous to G3086 194 G3771 PRT Glycine maxOrthologous to G3086 195 G3772 DNA Glycine max Predicted polypeptidesequence is orthologous to G3086 196 G3772 PRT Glycine max Orthologousto G3086 197 G3782 DNA Pinus taeda Predicted polypeptide sequence isorthologous to G3086 198 G3782 PRT Pinus taeda Orthologous to G3086 199G3794 DNA Zea mays Predicted polypeptide sequence is orthologous toG1792 200 G3794 PRT Zea mays Orthologous to G1792 201 G3795 DNA Capsicumannuum Predicted polypeptide sequence is orthologous to G1274 202 G3795PRT Capsicum annuum Orthologous to G1274 203 G3797 DNA Lactuca sativaPredicted polypeptide sequence is orthologous to G1274 204 G3797 PRTLactuca sativa Orthologous to G1274 205 G3802 DNA Sorghum bicolorPredicted polypeptide sequence is orthologous to G1274 206 G3802 PRTSorghum bicolor Orthologous to G1274 207 G3803 DNA Glycine max Predictedpolypeptide sequence is orthologous to G1274 208 G3803 PRT Glycine maxOrthologous to G1274 209 G3804 DNA Zea mays Predicted polypeptidesequence is orthologous to G1274 210 G3804 PRT Zea mays Orthologous toG1274 211 G3810 DNA Glycine max Predicted polypeptide sequence isorthologous to G922 212 G3810 PRT Glycine max Orthologous to G922 213G3811 DNA Glycine max Predicted polypeptide sequence is orthologous toG922 214 G3811 PRT Glycine max Orthologous to G922 215 G3813 DNA Oryzasativa Predicted polypeptide sequence is orthologous to G922 216 G3813PRT Oryza sativa Orthologous to G922 217 G3814 DNA Oryza sativaPredicted polypeptide sequence is orthologous to G922 218 G3814 PRTOryza sativa Orthologous to G922 219 G3824 DNA Lycopersicon Predictedpolypeptide sequence is esculentum orthologous to G922 220 G3824 PRTLycopersicon Orthologous to G922 esculentum 221 G3827 DNA Oryza sativaPredicted polypeptide sequence is orthologous to G922 222 G3827 PRTOryza sativa Orthologous to G922 223 G175 DNA Arabidopsis thalianaReference sequence 224 G175 PRT Arabidopsis thaliana Reference sequence225 G303 DNA Arabidopsis thaliana Reference sequence 226 G303 PRTArabidopsis thaliana Reference sequence 227 G354 DNA Arabidopsisthaliana Reference sequence 228 G354 PRT Arabidopsis thaliana Referencesequence 229 G489 DNA Arabidopsis thaliana Reference sequence 230 G489PRT Arabidopsis thaliana Reference sequence 231 G634 DNA Arabidopsisthaliana Reference sequence 232 G634 PRT Arabidopsis thaliana Referencesequence 233 G682 DNA Arabidopsis thaliana Reference sequence 234 G682PRT Arabidopsis thaliana Reference sequence 235 G916 DNA Arabidopsisthaliana Reference sequence 236 G916 PRT Arabidopsis thaliana Referencesequence 237 G975 DNA Arabidopsis thaliana Reference sequence; predictedpolypeptide sequence is paralogous to G2583 238 G975 PRT Arabidopsisthaliana Reference sequence; paralogous to G2583 239 G1069 DNAArabidopsis thaliana Reference sequence; functionally related,homologous to G1073 240 G1069 PRT Arabidopsis thaliana Referencesequence; functionally related, homologous to G1073 241 G1452 DNAArabidopsis thaliana Reference sequence; functionally related,homologous to G512 242 G1452 PRT Arabidopsis thaliana Referencesequence; functionally related, homologous to G512 243 G1820 DNAArabidopsis thaliana Reference sequence 244 G1820 PRT Arabidopsisthaliana Reference sequence 245 G2701 DNA Arabidopsis thaliana Referencesequence; predicted polypeptide sequence is paralogous to G1634 246G2701 PRT Arabidopsis thaliana Reference sequence; paralogous to G1634247 G2789 DNA Arabidopsis thaliana Reference sequence; predictedpolypeptide sequence is paralogous to G596 248 G2789 PRT Arabidopsisthaliana Reference sequence; paralogous to G596 249 G2839 DNAArabidopsis thaliana Reference sequence; predicted polypeptide sequenceis paralogous to G354 250 G2839 PRT Arabidopsis thaliana Referencesequence; paralogous to G354 251 G2854 DNA Arabidopsis thalianaReference sequence; predicted polypeptide sequence is paralogous toG1940 252 G2854 PRT Arabidopsis thaliana Reference sequence; paralogousto G1940 253 G3083 DNA Arabidopsis thaliana Reference sequence 254 G3083PRT Arabidopsis thaliana Reference sequence 255 G184 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G916 256 G184PRT Arabidopsis thaliana Paralogous to G916 257 G186 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G916 258 G186PRT Arabidopsis thaliana Paralogous to G916 259 G353 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G354 260 G353PRT Arabidopsis thaliana Paralogous to G354 261 G512 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G1452 262 G512PRT Arabidopsis thaliana Paralogous to G1452 263 G596 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2789 264 G596PRT Arabidopsis thaliana Paralogous to G2789 265 G714 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G489 266 G714PRT Arabidopsis thaliana Paralogous to G489 267 G877 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G175 268 G877PRT Arabidopsis thaliana Paralogous to G175 269 G1357 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G1452 270 G1357PRT Arabidopsis thaliana Paralogous to G1452 271 G1387 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G975 272 G1387PRT Arabidopsis thaliana Paralogous to G975 273 G1634 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2701 274 G1634PRT Arabidopsis thaliana Paralogous to G2701 275 G1889 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G354 276 G1889PRT Arabidopsis thaliana Paralogous to G354 277 G1940 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2854 278 G1940PRT Arabidopsis thaliana Paralogous to G2854 279 G1974 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G354 280 G1974PRT Arabidopsis thaliana Paralogous to G354 281 G2153 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G1073 282 G2153PRT Arabidopsis thaliana Paralogous to G1073 283 G2583 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G975 284 G2583PRT Arabidopsis thaliana Paralogous to G975 285 G226 DNA Arabidopsisthaliana Reference sequence; predicted polypeptide sequence isparalogous to G682 286 G226 PRT Arabidopsis thaliana Reference sequence;paralogous to G682 287 G481 DNA Arabidopsis thaliana Reference sequence;predicted polypeptide sequence is paralogous to G482 288 G481 PRTArabidopsis thaliana Reference sequence; paralogous to G482 289 G482 DNAArabidopsis thaliana Reference sequence; predicted polypeptide sequenceis paralogous to G481 290 G482 PRT Arabidopsis thaliana Referencesequence; paralogous to G481 291 G485 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G481 and G482 292 G485 PRTArabidopsis thaliana Paralogous to G481 and G482 293 G486 DNAArabidopsis thaliana Functionally related and homologous to G481 andG482 294 G486 PRT Arabidopsis thaliana Functionally related andhomologous to G481 and G482 295 G1067 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G1073 296 G1067 PRT Arabidopsisthaliana Paralogous to G1073 297 G1070 DNA Arabidopsis thalianaFunctionally related and homologous to G1073 298 G1070 PRT Arabidopsisthaliana Functionally related and homologous to G1073 299 G1073 DNAArabidopsis thaliana Reference sequence 300 G1073 PRT Arabidopsisthaliana Reference sequence 301 G1075 DNA Arabidopsis thalianaFunctionally related and homologous to G1073 302 G1075 PRT Arabidopsisthaliana Functionally related and homologous to G1073 303 G1076 DNAArabidopsis thaliana Functionally related and homologous to G1073 304G1076 PRT Arabidopsis thaliana Functionally related and homologous toG1073 305 G1248 DNA Arabidopsis thaliana Functionally related andhomologous to G481 and G482 306 G1248 PRT Arabidopsis thalianaFunctionally related and homologous to G481 and G482 307 G1364 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG481 and G482 308 G1364 PRT Arabidopsis thaliana Paralogous to G481 andG482 309 G1781 DNA Arabidopsis thaliana Functionally related andhomologous to G481 and G482 310 G1781 PRT Arabidopsis thalianaFunctionally related and homologous to G481 and G482 311 G1816 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG226 and G682 312 G1816 PRT Arabidopsis thaliana Paralogous to G226 andG682 313 G1945 DNA Arabidopsis thaliana Functionally related andhomologous to G1073 314 G1945 PRT Arabidopsis thaliana Functionallyrelated and homologous to G1073 315 G2155 DNA Arabidopsis thalianaFunctionally related and homologous to G1073 316 G2155 PRT Arabidopsisthaliana Functionally related and homologous to G1073 317 G2156 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG1073 318 G2156 PRT Arabidopsis thaliana Paralogous to G1073 319 G2345DNA Arabidopsis thaliana Predicted polypeptide sequence is paralogous toG481 and G482 320 G2345 PRT Arabidopsis thaliana Paralogous to G481 andG482 321 G2657 DNA Arabidopsis thaliana Functionally related andhomologous to G1073 322 G2657 PRT Arabidopsis thaliana Functionallyrelated and homologous to G1073 323 G2718 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G481 and G482 324 G2718PRT Arabidopsis thaliana Paralogous to G481 and G482 325 G3392 DNA Oryzasativa Predicted polypeptide sequence is orthologous to G682 326 G3392PRT Oryza sativa Orthologous to G682 327 G3393 DNA Oryza sativaPredicted polypeptide sequence is orthologous to G682 328 G3393 PRTOryza sativa Orthologous to G682 329 G3394 DNA Oryza sativa Predictedpolypeptide sequence is orthologous to G481 and G482 330 G3394 PRT Oryzasativa Orthologous to G481 and G482 331 G3395 DNA Oryza sativa Predictedpolypeptide sequence is orthologous to G481 and G482 332 G3395 PRT Oryzasativa Orthologous to G481 and G482 333 G3396 DNA Oryza sativa Predictedpolypeptide sequence is orthologous to G481 and G482 334 G3396 PRT Oryzasativa Orthologous to G481 and G482 335 G3397 DNA Oryza sativa Predictedpolypeptide sequence is orthologous to G481 and G482 336 G3397 PRT Oryzasativa Orthologous to G481 and G482 337 G3398 DNA Oryza sativa Predictedpolypeptide sequence is orthologous to G481 and G482 338 G3398 PRT Oryzasativa Orthologous to G481 and G482 339 G3399 DNA Oryza sativa Predictedpolypeptide sequence is orthologous to G1073 340 G3399 PRT Oryza sativaOrthologous to G1073 341 G3400 DNA Oryza sativa Predicted polypeptidesequence is orthologous to G1073 342 G3400 PRT Oryza sativa Orthologousto G1073 343 G3401 DNA Oryza sativa Predicted polypeptide sequence isorthologous to G1073 344 G3401 PRT Oryza sativa Orthologous to G1073 345G3403 DNA Oryza sativa Predicted polypeptide sequence is orthologous toG1073 346 G3403 PRT Oryza sativa Orthologous to G1073 347 G3404 DNAOryza sativa Functionally related and homologous to G1073 348 G3404 PRTOryza sativa Functionally related and homologous to G1073 349 G3405 DNAOryza sativa Functionally related and homologous to G1073 350 G3405 PRTOryza sativa Functionally related and homologous to G1073 351 G3406 DNAOryza sativa Functionally related and homologous to G1073 352 G3406 PRTOryza sativa Functionally related and homologous to G1073 353 G3407 DNAOryza sativa Functionally related and homologous to G1073 354 G3407 PRTOryza sativa Functionally related and homologous to G1073 355 G3408 DNAOryza sativa Functionally related and homologous to G1073 356 G3408 PRTOryza sativa Functionally related and homologous to G1073 357 G3429 DNAOryza sativa Predicted polypeptide sequence is orthologous to G481 andG482 358 G3429 PRT Oryza sativa Orthologous to G481 and G482 359 G3431DNA Zea mays Predicted polypeptide sequence is orthologous to G682 360G3431 PRT Zea mays Orthologous to G682 361 G3434 DNA Zea mays Predictedpolypeptide sequence is orthologous to G481 and G482 362 G3434 PRT Zeamays Orthologous to G481 and G482 363 G3435 DNA Zea mays Predictedpolypeptide sequence is orthologous to G481 and G482 364 G3435 PRT Zeamays Orthologous to G481 and G482 365 G3436 DNA Zea mays Predictedpolypeptide sequence is orthologous to G481 and G482 366 G3436 PRT Zeamays Orthologous to G481 and G482 367 G3437 DNA Zea mays Predictedpolypeptide sequence is orthologous to G481 and G482 368 G3437 PRT Zeamays Orthologous to G481 and G482 369 G3444 DNA Zea mays Predictedpolypeptide sequence is orthologous to G682 370 G3444 PRT Zea maysOrthologous to G682 371 G3445 DNA Glycine max Predicted polypeptidesequence is orthologous to G682 372 G3445 PRT Glycine max Orthologous toG682 373 G3446 DNA Glycine max Predicted polypeptide sequence isorthologous to G682 374 G3446 PRT Glycine max Orthologous to G682 375G3447 DNA Glycine max Predicted polypeptide sequence is orthologous toG682 376 G3447 PRT Glycine max Orthologous to G682 377 G3448 DNA Glycinemax Predicted polypeptide sequence is orthologous to G682 378 G3448 PRTGlycine max Orthologous to G682 379 G3449 DNA Glycine max Predictedpolypeptide sequence is orthologous to G682 380 G3449 PRT Glycine maxOrthologous to G682 381 G3450 DNA Glycine max Predicted polypeptidesequence is orthologous to G682 382 G3450 PRT Glycine max Orthologous toG682 383 G3456 DNA Glycine max Predicted polypeptide sequence isorthologous to G1073 384 G3456 PRT Glycine max Orthologous to G1073 385G3458 DNA Glycine max Functionally related and homologous to G1073 386G3458 PRT Glycine max Functionally related and homologous to G1073 387G3459 DNA Glycine max Predicted polypeptide sequence is functionallyrelated and homologous to G1073 388 G3459 PRT Glycine max Functionallyrelated and homologous to G1073 389 G3460 DNA Glycine max Predictedpolypeptide sequence is functionally related and homologous to G1073 390G3460 PRT Glycine max Functionally related and homologous to G1073 391G3462 DNA Glycine max Predicted polypeptide sequence is orthologous toG1073 392 G3462 PRT Glycine max Orthologous to G1073 393 G3470 DNAGlycine max Predicted polypeptide sequence is orthologous to G481 andG482 394 G3470 PRT Glycine max Orthologous to G481 and G482 395 G3471DNA Glycine max Predicted polypeptide sequence is orthologous to G481and G482 396 G3471 PRT Glycine max Orthologous to G481 and G482 397G3472 DNA Glycine max Predicted polypeptide sequence is orthologous toG481 and G482 398 G3472 PRT Glycine max Orthologous to G481 and G482 399G3473 DNA Glycine max Predicted polypeptide sequence is orthologous toG481 and G482 400 G3473 PRT Glycine max Orthologous to G481 and G482 401G3474 DNA Glycine max Predicted polypeptide sequence is orthologous toG481 and G482 402 G3474 PRT Glycine max Orthologous to G481 and G482 403G3475 DNA Glycine max Predicted polypeptide sequence is orthologous toG481 and G482 404 G3475 PRT Glycine max Orthologous to G481 and G482 405G3476 DNA Glycine max Predicted polypeptide sequence is orthologous toG481 and G482 406 G3476 PRT Glycine max Orthologous to G481 and G482 407G3477 DNA Glycine max Predicted polypeptide sequence is orthologous toG481 and G482 408 G3477 PRT Glycine max Orthologous to G481 and G482 409G3478 DNA Glycine max Predicted polypeptide sequence is orthologous toG481 and G482 410 G3478 PRT Glycine max Orthologous to G481 and G482 411G3556 DNA Oryza sativa Predicted polypeptide sequence is orthologous toG1073 412 G3556 PRT Oryza sativa Orthologous to G1073 413 G3835 DNAOryza sativa Predicted polypeptide sequence is orthologous to G481 andG482 414 G3835 PRT Oryza sativa Orthologous to G481 and G482 415 G3836DNA Oryza sativa Predicted polypeptide sequence is orthologous to G481and G482 416 G3836 PRT Oryza sativa Orthologous to G481 and G482 417G3837 DNA Glycine max Predicted polypeptide sequence is orthologous toG481 and G482 418 G3837 PRT Glycine max Orthologous to G481 and G482 419G24 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G12, G1277, G1379; orthologous to G3656 420 G24 PRTArabidopsis thaliana Paralogous to G12, G1277, G1379; orthologous toG3656 421 G154 DNA Arabidopsis thaliana Predicted polypeptide sequenceis paralogous to G1011 422 G154 PRT Arabidopsis thaliana Paralogous toG1011 423 G384 DNA Arabidopsis thaliana Predicted polypeptide sequenceis paralogous to G1588, G385 424 G384 PRT Arabidopsis thalianaParalogous to G1588, G385 425 G545 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G350, G351 426 G545 PRTArabidopsis thaliana Paralogous to G350, G351 427 G760 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G3041 428 G760PRT Arabidopsis thaliana Paralogous to G3041 429 G773 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G1412, G759 430G773 PRT Arabidopsis thaliana Paralogous to G1412, G759 433 G971 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG914 434 G971 PRT Arabidopsis thaliana Paralogous to G914 435 G988 DNAArabidopsis thaliana 436 G988 PRT Arabidopsis thaliana 441 G1322 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG221, G249 442 G1322 PRT Arabidopsis thaliana Paralogous to G221, G249449 G1818 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G1836 450 G1818 PRT Arabidopsis thaliana Paralogous toG1836 451 G1868 DNA Arabidopsis thaliana Predicted polypeptide sequenceis paralogous to G1439 452 G1868 PRT Arabidopsis thaliana Paralogous toG1439 453 G1888 DNA Arabidopsis thaliana Predicted polypeptide sequenceis paralogous to G1482 454 G1888 PRT Arabidopsis thaliana Paralogous toG1482 457 G2131 DNA Arabidopsis thaliana Predicted polypeptide sequenceis paralogous to G2106, G979 458 G2131 PRT Arabidopsis thalianaParalogous to G2106, G979 461 G2522 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G1071 462 G2522 PRT Arabidopsisthaliana Paralogous to G1071 465 G27 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G1386, G441 466 G27 PRTArabidopsis thaliana Paralogous to G1386, G441 471 G168 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G170, G2065 472G168 PRT Arabidopsis thaliana Paralogous to G170, G2065 479 G234 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG232 480 G234 PRT Arabidopsis thaliana Paralogous to G232 481 G237 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG1309 482 G237 PRT Arabidopsis thaliana Paralogous to G1309 483 G275 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG829, G837 484 G275 PRT Arabidopsis thaliana Paralogous to G829, G837485 G326 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G1337 486 G326 PRT Arabidopsis thaliana Paralogous toG1337 489 G427 DNA Arabidopsis thaliana Predicted polypeptide sequenceis paralogous to G2545, G425, G426 490 G427 PRT Arabidopsis thalianaParalogous to G2545, G425, G426 495 G602 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G1065 496 G602 PRTArabidopsis thaliana Paralogous to G1065 497 G618 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2057 498 G618PRT Arabidopsis thaliana Paralogous to G2057 503 G653 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G654 504 G653PRT Arabidopsis thaliana Paralogous to G654 507 G837 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G275, G829 508G837 PRT Arabidopsis thaliana Paralogous to G275, G829 509 G866 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG883 510 G866 PRT Arabidopsis thaliana Paralogous to G883 511 G872 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG2576; orthologous to G3652, G3653, G3654, G3655 512 G872 PRTArabidopsis thaliana Paralogous to G2576; orthologous to G3652, G3653,G3654, G3655 515 G912 DNA Arabidopsis thaliana Predicted polypeptidesequence is paralogous to G40, G2107, G2513, G41, G42; orthologous toG3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371, G3372, G3373,G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439, G3440, G3441,G3442, G3369, G3497, G3498, G3499, G3463, G3464, G3465, G3466, G3467,G3468, G3469 516 G912 PRT Arabidopsis thaliana Paralogous to G40, G2107,G2513, G41, G42; orthologous to G3362, G3364, G3365, G3366, G3367,G3368, G3370, G3371, G3372, G3373, G3374, G3375, G3376, G3377, G3378,G3379, G3438, G3439, G3440, G3441, G3442, G3369, G3497, G3498, G3499,G3463, G3464, G3465, G3466, G3467, G3468, G3469 517 G932 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G256, G666,G668; orthologous to G3384, G3385, G3386, G3500, G3501, G3502, G3537,G3538, G3539, G3540, G3541 518 G932 PRT Arabidopsis thaliana Paralogousto G256, G666, G668; orthologous to G3384, G3385, G3386, G3500, G3501,G3502, G3537, G3538, G3539, G3540, G3541 519 G958 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2180, G518 520G958 PRT Arabidopsis thaliana Paralogous to G2180, G518 521 G964 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG398, G399 522 G964 PRT Arabidopsis thaliana Paralogous to G398, G399523 G979 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G2106, G2131 524 G979 PRT Arabidopsis thaliana Paralogousto G2106, G2131 525 G1049 DNA Arabidopsis thaliana Predicted polypeptidesequence is paralogous to G572 526 G1049 PRT Arabidopsis thalianaParalogous to G572 529 G1255 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G1484 530 G1255 PRT Arabidopsisthaliana Paralogous to G1484 537 G1494 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G789 538 G1494 PRTArabidopsis thaliana Paralogous to G789 539 G1535 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G389 540 G1535PRT Arabidopsis thaliana Paralogous to G389 543 G1750 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G864, G440 544G1750 PRT Arabidopsis thaliana Paralogous to G864, G440 549 G1930 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG867, G9, G993; orthologous to G3388, G3389, G3390, G3391, G3432, G3433,G3451, G3452, G3453, G3454 550 G1930 PRT Arabidopsis thaliana Paralogousto G867, G9, G993; orthologous to G3388, G3389, G3390, G3391, G3432,G3433, G3451, G3452, G3453, G3454 551 G2057 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G618 552 G2057 PRTArabidopsis thaliana Paralogous to G618 553 G2144 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G1942 554 G2144PRT Arabidopsis thaliana Paralogous to G1942 555 G2145 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2148 556 G2145PRT Arabidopsis thaliana Paralogous to G2148 559 G2512 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G1752 560 G2512PRT Arabidopsis thaliana Paralogous to G1752 563 G2535 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G957, G961 564G2535 PRT Arabidopsis thaliana Paralogous to G957, G961 567 G2719 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG216 568 G2719 PRT Arabidopsis thaliana Paralogous to G216 569 G9 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG1930, G867, G993; orthologous to G3388, G3389, G3390, G3391, G3432,G3433, G3451, G3452, G3453, G3454 570 G9 PRT Arabidopsis thalianaParalogous to G1930, G867, G993; orthologous to G3388, G3389, G3390,G3391, G3432, G3433, G3451, G3452, G3453, G3454 571 G12 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G1277, G1379,G24; orthologous to G3656 572 G12 PRT Arabidopsis thaliana Paralogous toG1277, G1379, G24; orthologous to G3656 573 G40 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G2107, G2513, G41, G42,G912; orthologous to G3362, G3364, G3365, G3366, G3367, G3368, G3370,G3371, G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438,G3439, G3440, G3441, G3442, G3369, G3497, G3498, G3499, G3463, G3464,G3465, G3466, G3467, G3468, G3469 574 G40 PRT Arabidopsis thalianaParalogous to G2107, G2513, G41, G42, G912; orthologous to G3362, G3364,G3365, G3366, G3367, G3368, G3370, G3371, G3372, G3373, G3374, G3375,G3376, G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3369,G3497, G3498, G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 575G41 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G40, G2107, G2513, G42, G912; orthologous to G3362, G3364,G3365, G3366, G3367, G3368, G3370, G3371, G3372, G3373, G3374, G3375,G3376, G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3369,G3497, G3498, G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 576G41 PRT Arabidopsis thaliana Paralogous to G40, G2107, G2513, G42, G912;orthologous to G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371,G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439,G3440, G3441, G3442, G3369, G3497, G3498, G3499, G3463, G3464, G3465,G3466, G3467, G3468, G3469 577 G42 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G40, G2107, G2513, G41, G912;orthologous to G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371,G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439,G3440, G3441, G3442, G3369, G3497, G3498, G3499, G3463, G3464, G3465,G3466, G3467, G3468, G3469 578 G42 PRT Arabidopsis thaliana Paralogousto G40, G2107, G2513, G41, G912; orthologous to G3362, G3364, G3365,G3366, G3367, G3368, G3370, G3371, G3372, G3373, G3374, G3375, G3376,G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3369, G3497,G3498, G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 579 G170DNA Arabidopsis thaliana Predicted polypeptide sequence is paralogous toG168, G2065 580 G170 PRT Arabidopsis thaliana Paralogous to G168, G2065581 G216 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G2719 582 G216 PRT Arabidopsis thaliana Paralogous toG2719 583 G221 DNA Arabidopsis thaliana Predicted polypeptide sequenceis paralogous to G1322, G249 584 G221 PRT Arabidopsis thalianaParalogous to G1322, G249 585 G232 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G234 586 G232 PRT Arabidopsisthaliana Paralogous to G234 587 G249 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G1322, G221 588 G249 PRTArabidopsis thaliana Paralogous to G1322, G221 589 G256 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G666, G668,G932; orthologous to G3384, G3385, G3386, G3500, G3501, G3502, G3537,G3538, G3539, G3540, G3541 590 G256 PRT Arabidopsis thaliana Paralogousto G666, G668, G932; orthologous to G3384, G3385, G3386, G3500, G3501,G3502, G3537, G3538, G3539, G3540, G3541 591 G350 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G351, G545 592G350 PRT Arabidopsis thaliana Paralogous to G351, G545 593 G351 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG350, G545 594 G351 PRT Arabidopsis thaliana Paralogous to G350, G545595 G385 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G1588, G384 596 G385 PRT Arabidopsis thaliana Paralogousto G1588, G384 597 G389 DNA Arabidopsis thaliana Predicted polypeptidesequence is paralogous to G1535 598 G389 PRT Arabidopsis thalianaParalogous to G1535 599 G398 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G399, G964 600 G398 PRTArabidopsis thaliana Paralogous to G399, G964 601 G399 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G398, G964 602G399 PRT Arabidopsis thaliana Paralogous to G398, G964 603 G425 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG2545, G426, G427 604 G425 PRT Arabidopsis thaliana Paralogous to G2545,G426, G427 605 G426 DNA Arabidopsis thaliana Predicted polypeptidesequence is paralogous to G2545, G425, G427 606 G426 PRT Arabidopsisthaliana Paralogous to G2545, G425, G427 607 G440 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G864, G1750 608G440 PRT Arabidopsis thaliana Paralogous to G864, G1750 609 G441 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG1386, G27 610 G441 PRT Arabidopsis thaliana Paralogous to G1386, G27611 G518 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G2180, G958 612 G518 PRT Arabidopsis thaliana Paralogousto G2180, G958 613 G572 DNA Arabidopsis thaliana Predicted polypeptidesequence is paralogous to G1049 614 G572 PRT Arabidopsis thalianaParalogous to G1049 615 G654 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G653 616 G654 PRT Arabidopsisthaliana Paralogous to G653 617 G666 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G256, G668, G932; orthologous toG3384, G3385, G3386, G3500, G3501, G3502, G3537, G3538, G3539, G3540,G3541 618 G666 PRT Arabidopsis thaliana Paralogous to G256, G668, G932;orthologous to G3384, G3385, G3386, G3500, G3501, G3502, G3537, G3538,G3539, G3540, G3541 619 G668 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G256, G666, G932; orthologous toG3384, G3385, G3386, G3500, G3501, G3502, G3537, G3538, G3539, G3540,G3541 620 G668 PRT Arabidopsis thaliana Paralogous to G256, G666, G932;orthologous to G3384, G3385, G3386, G3500, G3501, G3502, G3537, G3538,G3539, G3540, G3541 621 G759 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G1412, G773 622 G759 PRTArabidopsis thaliana Paralogous to G1412, G773 623 G789 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G1494 624 G789PRT Arabidopsis thaliana Paralogous to G1494 625 G829 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G275, G837 626G829 PRT Arabidopsis thaliana Paralogous to G275, G837 627 G864 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG1750, G440 628 G864 PRT Arabidopsis thaliana Paralogous to G1750, G440629 G867 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G1930, G9, G993; orthologous to G3388, G3389, G3390,G3391, G3432, G3433, G3451, G3452, G3453, G3454 630 G867 PRT Arabidopsisthaliana Paralogous to G1930, G9, G993; orthologous to G3388, G3389,G3390, G3391, G3432, G3433, G3451, G3452, G3453, G3454 631 G883 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG866 632 G883 PRT Arabidopsis thaliana Paralogous to G866 633 G914 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG971 634 G914 PRT Arabidopsis thaliana Paralogous to G971 635 G957 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG2535, G961 636 G957 PRT Arabidopsis thaliana Paralogous to G2535, G961637 G961 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G2535, G957 638 G961 PRT Arabidopsis thaliana Paralogousto G2535, G957 639 G993 DNA Arabidopsis thaliana Predicted polypeptidesequence is paralogous to G1930, G867, G9; orthologous to G3388, G3389,G3390, G3391, G3432, G3433, G3451, G3452, G3453, G3454 640 G993 PRTArabidopsis thaliana Paralogous to G1930, G867, G9; orthologous toG3388, G3389, G3390, G3391, G3432, G3433, G3451, G3452, G3453, G3454 641G1011 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G154 642 G1011 PRT Arabidopsis thaliana Paralogous to G154643 G1065 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G602 644 G1065 PRT Arabidopsis thaliana Paralogous to G602645 G1071 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G2522 646 G1071 PRT Arabidopsis thaliana Paralogous toG2522 647 G1277 DNA Arabidopsis thaliana Predicted polypeptide sequenceis paralogous to G12, G1379, G24; orthologous to G3656 648 G1277 PRTArabidopsis thaliana Paralogous to G12, G1379, G24; orthologous to G3656649 G1309 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G237 650 G1309 PRT Arabidopsis thaliana Paralogous to G237651 G1337 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G326 652 G1337 PRT Arabidopsis thaliana Paralogous to G326653 G1379 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G12, G1277, G24; orthologous to G3656 654 G1379 PRTArabidopsis thaliana Paralogous to G12, G1277, G24; orthologous to G3656655 G1386 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G27, G441 656 G1386 PRT Arabidopsis thaliana Paralogous toG27, G441 657 G1412 DNA Arabidopsis thaliana Predicted polypeptidesequence is paralogous to G759, G773 658 G1412 PRT Arabidopsis thalianaParalogous to G759, G773 659 G1439 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G1868 660 G1439 PRT Arabidopsisthaliana Paralogous to G1868 661 G1482 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G1888 662 G1482 PRTArabidopsis thaliana Paralogous to G1888 663 G1484 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G1255 664 G1484PRT Arabidopsis thaliana Paralogous to G1255 665 G1588 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G384, G385 666G1588 PRT Arabidopsis thaliana Paralogous to G384, G385 667 G1752 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG2512 668 G1752 PRT Arabidopsis thaliana Paralogous to G2512 669 G1836DNA Arabidopsis thaliana Predicted polypeptide sequence is paralogous toG1818 670 G1836 PRT Arabidopsis thaliana Paralogous to G1818 671 G1942DNA Arabidopsis thaliana Predicted polypeptide sequence is paralogous toG2144 672 G1942 PRT Arabidopsis thaliana Paralogous to G2144 673 G2065DNA Arabidopsis thaliana Predicted polypeptide sequence is paralogous toG168, G170 674 G2065 PRT Arabidopsis thaliana Paralogous to G168, G170675 G2106 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G2131, G979 676 G2106 PRT Arabidopsis thaliana Paralogousto G2131, G979 677 G2107 DNA Arabidopsis thaliana Predicted polypeptidesequence is paralogous to G40, G2513, G41, G42, G912; orthologous toG3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371, G3372, G3373,G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439, G3440, G3441,G3442, G3369, G3497, G3498, G3499, G3463, G3464, G3465, G3466, G3467,G3468, G3469 678 G2107 PRT Arabidopsis thaliana Paralogous to G40,G2513, G41, G42, G912; orthologous to G3362, G3364, G3365, G3366, G3367,G3368, G3370, G3371, G3372, G3373, G3374, G3375, G3376, G3377, G3378,G3379, G3438, G3439, G3440, G3441, G3442, G3369, G3497, G3498, G3499,G3463, G3464, G3465, G3466, G3467, G3468, G3469 679 G2148 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG2145 680 G2148 PRT Arabidopsis thaliana Paralogous to G2145 681 G2180DNA Arabidopsis thaliana Predicted polypeptide sequence is paralogous toG518, G958 682 G2180 PRT Arabidopsis thaliana Paralogous to G518, G958683 G2513 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G40, G2107, G41, G42, G912; orthologous to G3362, G3364,G3365, G3366, G3367, G3368, G3370, G3371, G3372, G3373, G3374, G3375,G3376, G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3369,G3497, G3498, G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 684G2513 PRT Arabidopsis thaliana Paralogous to G40, G2107, G41, G42, G912;orthologous to G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371,G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439,G3440, G3441, G3442, G3369, G3497, G3498, G3499, G3463, G3464, G3465,G3466, G3467, G3468, G3469 685 G2545 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G425, G426, G427 686 G2545 PRTArabidopsis thaliana Paralogous to G425, G426, G427 687 G2576 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG872; orthologous to G3652, G3653, G3654, G3655 688 G2576 PRTArabidopsis thaliana Paralogous to G872; orthologous to G3652, G3653,G3654, G3655 689 G3041 DNA Arabidopsis thaliana Predicted polypeptidesequence is paralogous to G760 690 G3041 PRT Arabidopsis thalianaParalogous to G760 691 G3362 DNA Medicago truncatula Predictedpolypeptide sequence is paralogous to G3364, G3365, G3366, G3367, G3368,G3369; orthologous to G40, G2107, G2513, G41, G42, G912, G3370, G3371,G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439,G3440, G3441, G3442, G3497, G3498, G3499, G3463, G3464, G3465, G3466,G3467, G3468, G3469 692 G3362 PRT Medicago truncatula Paralogous toG3364, G3365, G3366, G3367, G3368, G3369; orthologous to G40, G2107,G2513, G41, G42, G912, G3370, G3371, G3372, G3373, G3374, G3375, G3376,G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3497, G3498,G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 693 G3364 DNAMedicago truncatula Predicted polypeptide sequence is paralogous toG3362, G3365, G3366, G3367, G3368, G3369; orthologous to G40, G2107,G2513, G41, G42, G912, G3370, G3371, G3372, G3373, G3374, G3375, G3376,G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3497, G3498,G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 694 G3364 PRTMedicago truncatula Paralogous to G3362, G3365, G3366, G3367, G3368,G3369; orthologous to G40, G2107, G2513, G41, G42, G912, G3370, G3371,G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439,G3440, G3441, G3442, G3497, G3498, G3499, G3463, G3464, G3465, G3466,G3467, G3468, G3469 695 G3365 DNA Medicago truncatula Predictedpolypeptide sequence is paralogous to G3362, G3364, G3366, G3367, G3368,G3369; orthologous to G40, G2107, G2513, G41, G42, G912, G3370, G3371,G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439,G3440, G3441, G3442, G3497, G3498, G3499, G3463, G3464, G3465, G3466,G3467, G3468, G3469 696 G3365 PRT Medicago truncatula Paralogous toG3362, G3364, G3366, G3367, G3368, G3369; orthologous to G40, G2107,G2513, G41, G42, G912, G3370, G3371, G3372, G3373, G3374, G3375, G3376,G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3497, G3498,G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 697 G3366 DNAMedicago truncatula Predicted polypeptide sequence is paralogous toG3362, G3364, G3365, G3367, G3368, G3369; orthologous to G40, G2107,G2513, G41, G42, G912, G3370, G3371, G3372, G3373, G3374, G3375, G3376,G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3497, G3498,G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 698 G3366 PRTMedicago truncatula Paralogous to G3362, G3364, G3365, G3367, G3368,G3369; orthologous to G40, G2107, G2513, G41, G42, G912, G3370, G3371,G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439,G3440, G3441, G3442, G3497, G3498, G3499, G3463, G3464, G3465, G3466,G3467, G3468, G3469 699 G3367 DNA Medicago truncatula Predictedpolypeptide sequence is paralogous to G3362, G3364, G3365, G3366, G3368,G3369; orthologous to G40, G2107, G2513, G41, G42, G912, G3370, G3371,G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439,G3440, G3441, G3442, G3497, G3498, G3499, G3463, G3464, G3465, G3466,G3467, G3468, G3469 700 G3367 PRT Medicago truncatula Paralogous toG3362, G3364, G3365, G3366, G3368, G3369; orthologous to G40, G2107,G2513, G41, G42, G912, G3370, G3371, G3372, G3373, G3374, G3375, G3376,G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3497, G3498,G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 701 G3368 DNAMedicago truncatula Predicted polypeptide sequence is paralogous toG3362, G3364, G3365, G3366, G3367, G3369; orthologous to G40, G2107,G2513, G41, G42, G912, G3370, G3371, G3372, G3373, G3374, G3375, G3376,G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3497, G3498,G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 702 G3368 PRTMedicago truncatula Paralogous to G3362, G3364, G3365, G3366, G3367,G3369; orthologous to G40, G2107, G2513, G41, G42, G912, G3370, G3371,G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439,G3440, G3441, G3442, G3497, G3498, G3499, G3463, G3464, G3465, G3466,G3467, G3468, G3469 703 G3369 DNA Medicago truncatula Predictedpolypeptide sequence is paralogous to G3362, G3364, G3365, G3366, G3367,G3368; orthologous to G40, G2107, G2513, G41, G42, G912, G3370, G3371,G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439,G3440, G3441, G3442, G3497, G3498, G3499, G3463, G3464, G3465, G3466,G3467, G3468, G3469 704 G3369 PRT Medicago truncatula Paralogous toG3362, G3364, G3365, G3366, G3367, G3368; orthologous to G40, G2107,G2513, G41, G42, G912, G3370, G3371, G3372, G3373, G3374, G3375, G3376,G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3497, G3498,G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 705 G3370 DNAOryza sativa Predicted polypeptide sequence is paralogous to G3371,G3374, G3376, G3378; orthologous to G40, G2107, G2513, G41, G42, G912,G3362, G3364, G3365, G3366, G3367, G3368, G3372, G3373, G3375, G3377,G3379, G3438, G3439, G3440, G3441, G3442, G3369, G3497, G3498, G3499,G3463, G3464, G3465, G3466, G3467, G3468, G3469 706 G3370 PRT Oryzasativa Paralogous to G3371, G3374, G3376, G3378; orthologous to G40,G2107, G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367, G3368,G3372, G3373, G3375, G3377, G3379, G3438, G3439, G3440, G3441, G3442,G3369, G3497, G3498, G3499, G3463, G3464, G3465, G3466, G3467, G3468,G3469 707 G3371 DNA Oryza sativa Predicted polypeptide sequence isparalogous to G3370, G3374, G3376, G3378; orthologous to G40, G2107,G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367, G3368, G3372,G3373, G3375, G3377, G3379, G3438, G3439, G3440, G3441, G3442, G3369,G3497, G3498, G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 708G3371 PRT Oryza sativa Paralogous to G3370, G3374, G3376, G3378;orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365,G3366, G3367, G3368, G3372, G3373, G3375, G3377, G3379, G3438, G3439,G3440, G3441, G3442, G3369, G3497, G3498, G3499, G3463, G3464, G3465,G3466, G3467, G3468, G3469 709 G3372 DNA Oryza sativa Predictedpolypeptide sequence is paralogous to G3373, G3375, G3377, G3379;orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365,G3366, G3367, G3368, G3370, G3371, G3374, G3376, G3378, G3438, G3439,G3440, G3441, G3442, G3369, G3497, G3498, G3499, G3463, G3464, G3465,G3466, G3467, G3468, G3469 710 G3372 PRT Oryza sativa Paralogous toG3373, G3375, G3377, G3379; orthologous to G40, G2107, G2513, G41, G42,G912, G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371, G3374,G3376, G3378, G3438, G3439, G3440, G3441, G3442, G3369, G3497, G3498,G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 711 G3373 DNAOryza sativa Predicted polypeptide sequence is paralogous to G3372,G3375, G3377, G3379; orthologous to G40, G2107, G2513, G41, G42, G912,G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371, G3374, G3376,G3378, G3438, G3439, G3440, G3441, G3442, G3369, G3497, G3498, G3499,G3463, G3464, G3465, G3466, G3467, G3468, G3469 712 G3373 PRT Oryzasativa Paralogous to G3372, G3375, G3377, G3379; orthologous to G40,G2107, G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367, G3368,G3370, G3371, G3374, G3376, G3378, G3438, G3439, G3440, G3441, G3442,G3369, G3497, G3498, G3499, G3463, G3464, G3465, G3466, G3467, G3468,G3469 713 G3374 DNA Oryza sativa Predicted polypeptide sequence isparalogous to G3370, G3371, G3376, G3378; orthologous to G40, G2107,G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367, G3368, G3372,G3373, G3375, G3377, G3379, G3438, G3439, G3440, G3441, G3442, G3369,G3497, G3498, G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 714G3374 PRT Oryza sativa Paralogous to G3370, G3371, G3376, G3378;orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365,G3366, G3367, G3368, G3372, G3373, G3375, G3377, G3379, G3438, G3439,G3440, G3441, G3442, G3369, G3497, G3498, G3499, G3463, G3464, G3465,G3466, G3467, G3468, G3469 715 G3375 DNA Oryza sativa Predictedpolypeptide sequence is paralogous to G3372, G3373, G3377, G3379;orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365,G3366, G3367, G3368, G3370, G3371, G3374, G3376, G3378, G3438, G3439,G3440, G3441, G3442, G3369, G3497, G3498, G3499, G3463, G3464, G3465,G3466, G3467, G3468, G3469 716 G3375 PRT Oryza sativa Paralogous toG3372, G3373, G3377, G3379; orthologous to G40, G2107, G2513, G41, G42,G912, G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371, G3374,G3376, G3378, G3438, G3439, G3440, G3441, G3442, G3369, G3497, G3498,G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 717 G3376 DNAOryza sativa Predicted polypeptide sequence is paralogous to G3370,G3371, G3374, G3378; orthologous to G40, G2107, G2513, G41, G42, G912,G3362, G3364, G3365, G3366, G3367, G3368, G3372, G3373, G3375, G3377,G3379, G3438, G3439, G3440, G3441, G3442, G3369, G3497, G3498, G3499,G3463, G3464, G3465, G3466, G3467, G3468, G3469 718 G3376 PRT Oryzasativa Paralogous to G3370, G3371, G3374, G3378; orthologous to G40,G2107, G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367, G3368,G3372, G3373, G3375, G3377, G3379, G3438, G3439, G3440, G3441, G3442,G3369, G3497, G3498, G3499, G3463, G3464, G3465, G3466, G3467, G3468,G3469 719 G3377 DNA Oryza sativa Predicted polypeptide sequence isparalogous to G3372, G3373, G3375, G3379; orthologous to G40, G2107,G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367, G3368, G3370,G3371, G3374, G3376, G3378, G3438, G3439, G3440, G3441, G3442, G3369,G3497, G3498, G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 720G3377 PRT Oryza sativa Paralogous to G3372, G3373, G3375, G3379;orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365,G3366, G3367, G3368, G3370, G3371, G3374, G3376, G3378, G3438, G3439,G3440, G3441, G3442, G3369, G3497, G3498, G3499, G3463, G3464, G3465,G3466, G3467, G3468, G3469 721 G3378 DNA Oryza sativa Predictedpolypeptide sequence is paralogous to G3370, G3371, G3374, G3376;orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365,G3366, G3367, G3368, G3372, G3373, G3375, G3377, G3379, G3438, G3439,G3440, G3441, G3442, G3369, G3497, G3498, G3499, G3463, G3464, G3465,G3466, G3467, G3468, G3469 722 G3378 PRT Oryza sativa Paralogous toG3370, G3371, G3374, G3376; orthologous to G40, G2107, G2513, G41, G42,G912, G3362, G3364, G3365, G3366, G3367, G3368, G3372, G3373, G3375,G3377, G3379, G3438, G3439, G3440, G3441, G3442, G3369, G3497, G3498,G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 723 G3379 DNAOryza sativa Predicted polypeptide sequence is paralogous to G3372,G3373, G3375, G3377; orthologous to G40, G2107, G2513, G41, G42, G912,G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371, G3374, G3376,G3378, G3438, G3439, G3440, G3441, G3442, G3369, G3497, G3498, G3499,G3463, G3464, G3465, G3466, G3467, G3468, G3469 724 G3379 PRT Oryzasativa Paralogous to G3372, G3373, G3375, G3377; orthologous to G40,G2107, G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367, G3368,G3370, G3371, G3374, G3376, G3378, G3438, G3439, G3440, G3441, G3442,G3369, G3497, G3498, G3499, G3463, G3464, G3465, G3466, G3467, G3468,G3469 725 G3384 DNA Oryza sativa Predicted polypeptide sequence isparalogous to G3385, G3386, G3502; orthologous to G256, G666, G668,G932, G3500, G3501, G3537, G3538, G3539, G3540, G3541 726 G3384 PRTOryza sativa Paralogous to G3385, G3386, G3502; orthologous to G256,G666, G668, G932, G3500, G3501, G3537, G3538, G3539, G3540, G3541 727G3385 DNA Oryza sativa Predicted polypeptide sequence is paralogous toG3384, G3386, G3502; orthologous to G256, G666, G668, G932, G3500,G3501, G3537, G3538, G3539, G3540, G3541 728 G3385 PRT Oryza sativaParalogous to G3384, G3386, G3502; orthologous to G256, G666, G668,G932, G3500, G3501, G3537, G3538, G3539, G3540, G3541 729 G3386 DNAOryza sativa Predicted polypeptide sequence is paralogous to G3384,G3385, G3502; orthologous to G256, G666, G668, G932, G3500, G3501,G3537, G3538, G3539, G3540, G3541 730 G3386 PRT Oryza sativa Paralogousto G3384, G3385, G3502; orthologous to G256, G666, G668, G932, G3500,G3501, G3537, G3538, G3539, G3540, G3541 731 G3388 DNA Oryza sativaPredicted polypeptide sequence is paralogous to G3389, G3390, G3391;orthologous to G1930, G867, G9, G993, G3432, G3433, G3451, G3452, G3453,G3454 732 G3388 PRT Oryza sativa Paralogous to G3389, G3390, G3391;orthologous to G1930, G867, G9, G993, G3432, G3433, G3451, G3452, G3453,G3454 733 G3389 DNA Oryza sativa Predicted polypeptide sequence isparalogous to G3388, G3390, G3391; orthologous to G1930, G867, G9, G993,G3432, G3433, G3451, G3452, G3453, G3454 734 G3389 PRT Oryza sativaParalogous to G3388, G3390, G3391; orthologous to G1930, G867, G9, G993,G3432, G3433, G3451, G3452, G3453, G3454 735 G3390 DNA Oryza sativaPredicted polypeptide sequence is paralogous to G3388, G3389, G3391;orthologous to G1930, G867, G9, G993, G3432, G3433, G3451, G3452, G3453,G3454 736 G3390 PRT Oryza sativa Paralogous to G3388, G3389, G3391;orthologous to G1930, G867, G9, G993, G3432, G3433, G3451, G3452, G3453,G3454 737 G3391 DNA Oryza sativa Predicted polypeptide sequence isparalogous to G3388, G3389, G3390; orthologous to G1930, G867, G9, G993,G3432, G3433, G3451, G3452, G3453, G3454 738 G3391 PRT Oryza sativaParalogous to G3388, G3389, G3390; orthologous to G1930, G867, G9, G993,G3432, G3433, G3451, G3452, G3453, G3454 739 G3432 DNA Zea maysPredicted polypeptide sequence is paralogous to G3433; orthologous toG1930, G867, G9, G993, G3388, G3389, G3390, G3391, G3451, G3452, G3453,G3454 740 G3432 PRT Zea mays Paralogous to G3433; orthologous to G1930,G867, G9, G993, G3388, G3389, G3390, G3391, G3451, G3452, G3453, G3454741 G3433 DNA Zea mays Predicted polypeptide sequence is paralogous toG3432; orthologous to G1930, G867, G9, G993, G3388, G3389, G3390, G3391,G3451, G3452, G3453, G3454 742 G3433 PRT Zea mays Paralogous to G3432;orthologous to G1930, G867, G9, G993, G3388, G3389, G3390, G3391, G3451,G3452, G3453, G3454 743 G3438 DNA Zea mays Predicted polypeptidesequence is paralogous to G3439, G3440, G3441, G3442; orthologous toG40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367,G3368, G3370, G3371, G3372, G3373, G3374, G3375, G3376, G3377, G3378,G3379, G3369, G3497, G3498, G3499, G3463, G3464, G3465, G3466, G3467,G3468, G3469 744 G3438 PRT Zea mays Paralogous to G3439, G3440, G3441,G3442; orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364,G3365, G3366, G3367, G3368, G3370, G3371, G3372, G3373, G3374, G3375,G3376, G3377, G3378, G3379, G3369, G3497, G3498, G3499, G3463, G3464,G3465, G3466, G3467, G3468, G3469 745 G3439 DNA Zea mays Predictedpolypeptide sequence is paralogous to G3438, G3440, G3441, G3442;orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365,G3366, G3367, G3368, G3370, G3371, G3372, G3373, G3374, G3375, G3376,G3377, G3378, G3379, G3369, G3497, G3498, G3499, G3463, G3464, G3465,G3466, G3467, G3468, G3469 746 G3439 PRT Zea mays Paralogous to G3438,G3440, G3441, G3442; orthologous to G40, G2107, G2513, G41, G42, G912,G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371, G3372, G3373,G3374, G3375, G3376, G3377, G3378, G3379, G3369, G3497, G3498, G3499,G3463, G3464, G3465, G3466, G3467, G3468, G3469 747 G3440 DNA Zea maysPredicted polypeptide sequence is paralogous to G3438, G3439, G3441,G3442; orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364,G3365, G3366, G3367, G3368, G3370, G3371, G3372, G3373, G3374, G3375,G3376, G3377, G3378, G3379, G3369, G3497, G3498, G3499, G3463, G3464,G3465, G3466, G3467, G3468, G3469 748 G3440 PRT Zea mays Paralogous toG3438, G3439, G3441, G3442; orthologous to G40, G2107, G2513, G41, G42,G912, G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371, G3372,G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3369, G3497, G3498,G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 749 G3441 DNA Zeamays Predicted polypeptide sequence is paralogous to G3438, G3439,G3440, G3442; orthologous to G40, G2107, G2513, G41, G42, G912, G3362,G3364, G3365, G3366, G3367, G3368, G3370, G3371, G3372, G3373, G3374,G3375, G3376, G3377, G3378, G3379, G3369, G3497, G3498, G3499, G3463,G3464, G3465, G3466, G3467, G3468, G3469 750 G3441 PRT Zea maysParalogous to G3438, G3439, G3440, G3442; orthologous to G40, G2107,G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367, G3368, G3370,G3371, G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3369,G3497, G3498, G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 751G3442 DNA Zea mays Predicted polypeptide sequence is paralogous toG3438, G3439, G3440, G3441; orthologous to G40, G2107, G2513, G41, G42,G912, G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371, G3372,G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3369, G3497, G3498,G3499, G3463, G3464, G3465, G3466, G3467, G3468, G3469 752 G3442 PRT Zeamays Paralogous to G3438, G3439, G3440, G3441; orthologous to G40,G2107, G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367, G3368,G3370, G3371, G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379,G3369, G3497, G3498, G3499, G3463, G3464, G3465, G3466, G3467, G3468,G3469 753 G3451 DNA Glycine max Predicted polypeptide sequence isparalogous to G3452, G3453, G3454; orthologous to G1930, G867, G9, G993,G3388, G3389, G3390, G3391, G3432, G3433 754 G3451 PRT Glycine maxParalogous to G3452, G3453, G3454; orthologous to G1930, G867, G9, G993,G3388, G3389, G3390, G3391, G3432, G3433 755 G3452 DNA Glycine maxPredicted polypeptide sequence is paralogous to G3451, G3453, G3454;orthologous to G1930, G867, G9, G993, G3388, G3389, G3390, G3391, G3432,G3433 756 G3452 PRT Glycine max Paralogous to G3451, G3453, G3454;orthologous to G1930, G867, G9, G993, G3388, G3389, G3390, G3391, G3432,G3433 757 G3453 DNA Glycine max Predicted polypeptide sequence isparalogous to G3451, G3452, G3454; orthologous to G1930, G867, G9, G993,G3388, G3389, G3390, G3391, G3432, G3433 758 G3453 PRT Glycine maxParalogous to G3451, G3452, G3454; orthologous to G1930, G867, G9, G993,G3388, G3389, G3390, G3391, G3432, G3433 759 G3454 DNA Glycine maxPredicted polypeptide sequence is paralogous to G3451, G3452, G3453;orthologous to G1930, G867, G9, G993, G3388, G3389, G3390, G3391, G3432,G3433 760 G3454 PRT Glycine max Paralogous to G3451, G3452, G3453;orthologous to G1930, G867, G9, G993, G3388, G3389, G3390, G3391, G3432,G3433 761 G3463 DNA Glycine max Predicted polypeptide sequence isparalogous to G3464, G3465, G3466, G3467, G3468, G3469; orthologous toG40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367,G3368, G3370, G3371, G3372, G3373, G3374, G3375, G3376, G3377, G3378,G3379, G3438, G3439, G3440, G3441, G3442, G3369, G3497, G3498, G3499 762G3463 PRT Glycine max Paralogous to G3464, G3465, G3466, G3467, G3468,G3469; orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364,G3365, G3366, G3367, G3368, G3370, G3371, G3372, G3373, G3374, G3375,G3376, G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3369,G3497, G3498, G3499 763 G3464 DNA Glycine max Predicted polypeptidesequence is paralogous to G3463, G3465, G3466, G3467, G3468, G3469;orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365,G3366, G3367, G3368, G3370, G3371, G3372, G3373, G3374, G3375, G3376,G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3369, G3497,G3498, G3499 764 G3464 PRT Glycine max Paralogous to G3463, G3465,G3466, G3467, G3468, G3469; orthologous to G40, G2107, G2513, G41, G42,G912, G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371, G3372,G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439, G3440,G3441, G3442, G3369, G3497, G3498, G3499 765 G3465 DNA Glycine maxPredicted polypeptide sequence is paralogous to G3463, G3464, G3466,G3467, G3468, G3469; orthologous to G40, G2107, G2513, G41, G42, G912,G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371, G3372, G3373,G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439, G3440, G3441,G3442, G3369, G3497, G3498, G3499 766 G3465 PRT Glycine max Paralogousto G3463, G3464, G3466, G3467, G3468, G3469; orthologous to G40, G2107,G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367, G3368, G3370,G3371, G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438,G3439, G3440, G3441, G3442, G3369, G3497, G3498, G3499 767 G3466 DNAGlycine max Predicted polypeptide sequence is paralogous to G3463,G3464, G3465, G3467, G3468, G3469; orthologous to G40, G2107, G2513,G41, G42, G912, G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371,G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439,G3440, G3441, G3442, G3369, G3497, G3498, G3499 768 G3466 PRT Glycinemax Paralogous to G3463, G3464, G3465, G3467, G3468, G3469; orthologousto G40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367,G3368, G3370, G3371, G3372, G3373, G3374, G3375, G3376, G3377, G3378,G3379, G3438, G3439, G3440, G3441, G3442, G3369, G3497, G3498, G3499 769G3467 DNA Glycine max Predicted polypeptide sequence is paralogous toG3463, G3464, G3465, G3466, G3468, G3469; orthologous to G40, G2107,G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367, G3368, G3370,G3371, G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438,G3439, G3440, G3441, G3442, G3369, G3497, G3498, G3499 770 G3467 PRTGlycine max Paralogous to G3463, G3464, G3465, G3466, G3468, G3469;orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365,G3366, G3367, G3368, G3370, G3371, G3372, G3373, G3374, G3375, G3376,G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3369, G3497,G3498, G3499 771 G3468 DNA Glycine max Predicted polypeptide sequence isparalogous to G3463, G3464, G3465, G3466, G3467, G3469; orthologous toG40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367,G3368, G3370, G3371, G3372, G3373, G3374, G3375, G3376, G3377, G3378,G3379, G3438, G3439, G3440, G3441, G3442, G3369, G3497, G3498, G3499 772G3468 PRT Glycine max Paralogous to G3463, G3464, G3465, G3466, G3467,G3469; orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364,G3365, G3366, G3367, G3368, G3370, G3371, G3372, G3373, G3374, G3375,G3376, G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3369,G3497, G3498, G3499 773 G3469 DNA Glycine max Predicted polypeptidesequence is paralogous to G3463, G3464, G3465, G3466, G3467, G3468;orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365,G3366, G3367, G3368, G3370, G3371, G3372, G3373, G3374, G3375, G3376,G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3369, G3497,G3498, G3499 774 G3469 PRT Glycine max Paralogous to G3463, G3464,G3465, G3466, G3467, G3468; orthologous to G40, G2107, G2513, G41, G42,G912, G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371, G3372,G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439, G3440,G3441, G3442, G3369, G3497, G3498, G3499 775 G3497 DNA Medicago sativaPredicted polypeptide sequence is paralogous to G3498, G3499;orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365,G3366, G3367, G3368, G3370, G3371, G3372, G3373, G3374, G3375, G3376,G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3369, G3463,G3464, G3465, G3466, G3467, G3468, G3469 776 G3497 PRT Medicago sativaParalogous to G3498, G3499; orthologous to G40, G2107, G2513, G41, G42,G912, G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371, G3372,G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439, G3440,G3441, G3442, G3369, G3463, G3464, G3465, G3466, G3467, G3468, G3469 777G3498 DNA Medicago sativa Predicted polypeptide sequence is paralogousto G3497, G3499; orthologous to G40, G2107, G2513, G41, G42, G912,G3362, G3364, G3365, G3366, G3367, G3368, G3370, G3371, G3372, G3373,G3374, G3375, G3376, G3377, G3378, G3379, G3438, G3439, G3440, G3441,G3442, G3369, G3463, G3464, G3465, G3466, G3467, G3468, G3469 778 G3498PRT Medicago sativa Paralogous to G3497, G3499; orthologous to G40,G2107, G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367, G3368,G3370, G3371, G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379,G3438, G3439, G3440, G3441, G3442, G3369, G3463, G3464, G3465, G3466,G3467, G3468, G3469 779 G3499 DNA Medicago sativa Predicted polypeptidesequence is paralogous to G3497, G3498; orthologous to G40, G2107,G2513, G41, G42, G912, G3362, G3364, G3365, G3366, G3367, G3368, G3370,G3371, G3372, G3373, G3374, G3375, G3376, G3377, G3378, G3379, G3438,G3439, G3440, G3441, G3442, G3369, G3463, G3464, G3465, G3466, G3467,G3468, G3469 780 G3499 PRT Medicago sativa Paralogous to G3497, G3498;orthologous to G40, G2107, G2513, G41, G42, G912, G3362, G3364, G3365,G3366, G3367, G3368, G3370, G3371, G3372, G3373, G3374, G3375, G3376,G3377, G3378, G3379, G3438, G3439, G3440, G3441, G3442, G3369, G3463,G3464, G3465, G3466, G3467, G3468, G3469 781 G3500 DNA LycopersiconPredicted polypeptide sequence is esculentum paralogous to G3501;orthologous to G256, G666, G668, G932, G3384, G3385, G3386, G3502,G3537, G3538, G3539, G3540, G3541 782 G3500 PRT Lycopersicon Paralogousto G3501; orthologous to esculentum G256, G666, G668, G932, G3384,G3385, G3386, G3502, G3537, G3538, G3539, G3540, G3541 783 G3501 DNALycopersicon Predicted polypeptide sequence is esculentum paralogous toG3500; orthologous to G256, G666, G668, G932, G3384, G3385, G3386,G3502, G3537, G3538, G3539, G3540, G3541 784 G3501 PRT LycopersiconParalogous to G3500; orthologous to esculentum G256, G666, G668, G932,G3384, G3385, G3386, G3502, G3537, G3538, G3539, G3540, G3541 785 G3502DNA Oryza sativa Predicted polypeptide sequence is paralogous to G3384,G3385, G3386; orthologous to G256, G666, G668, G932, G3500, G3501,G3537, G3538, G3539, G3540, G3541 786 G3502 PRT Oryza sativa Paralogousto G3384, G3385, G3386; orthologous to G256, G666, G668, G932, G3500,G3501, G3537, G3538, G3539, G3540, G3541 787 G3537 DNA Glycine maxPredicted polypeptide sequence is paralogous to G3538, G3539;orthologous to G256, G666, G668, G932, G3384, G3385, G3386, G3500,G3501, G3502, G3540, G3541 788 G3537 PRT Glycine max Paralogous toG3538, G3539; orthologous to G256, G666, G668, G932, G3384, G3385,G3386, G3500, G3501, G3502, G3540, G3541 789 G3538 DNA Glycine maxPredicted polypeptide sequence is paralogous to G3537, G3539;orthologous to G256, G666, G668, G932, G3384, G3385, G3386, G3500,G3501, G3502, G3540, G3541 790 G3538 PRT Glycine max Paralogous toG3537, G3539; orthologous to G256, G666, G668, G932, G3384, G3385,G3386, G3500, G3501, G3502, G3540, G3541 791 G3539 DNA Glycine maxPredicted polypeptide sequence is paralogous to G3537, G3538;orthologous to G256, G666, G668, G932, G3384, G3385, G3386, G3500,G3501, G3502, G3540, G3541 792 G3539 PRT Glycine max Paralogous toG3537, G3538; orthologous to G256, G666, G668, G932, G3384, G3385,G3386, G3500, G3501, G3502, G3540, G3541 793 G3540 DNA Zea maysPredicted polypeptide sequence is paralogous to G3541; orthologous toG256, G666, G668, G932, G3384, G3385, G3386, G3500, G3501, G3502, G3537,G3538, G3539 794 G3540 PRT Zea mays Paralogous to G3541; orthologous toG256, G666, G668, G932, G3384, G3385, G3386, G3500, G3501, G3502, G3537,G3538, G3539 795 G3541 DNA Zea mays Predicted polypeptide sequence isparalogous to G3540; orthologous to G256, G666, G668, G932, G3384,G3385, G3386, G3500, G3501, G3502, G3537, G3538, G3539 796 G3541 PRT Zeamays Paralogous to G3540; orthologous to G256, G666, G668, G932, G3384,G3385, G3386, G3500, G3501, G3502, G3537, G3538, G3539 797 G3652 DNAOryza sativa Predicted polypeptide sequence is paralogous to G3653,G3654, G3655; orthologous to G2576, G872 798 G3652 PRT Oryza sativaParalogous to G3653, G3654, G3655; orthologous to G2576, G872 799 G3653DNA Oryza sativa Predicted polypeptide sequence is paralogous to G3652,G3654, G3655; orthologous to G2576, G872 800 G3653 PRT Oryza sativaParalogous to G3652, G3654, G3655; orthologous to G2576, G872 801 G3654DNA Oryza sativa Predicted polypeptide sequence is paralogous to G3652,G3653, G3655; orthologous to G2576, G872 802 G3654 PRT Oryza sativaParalogous to G3652, G3653, G3655; orthologous to G2576, G872 803 G3655DNA Oryza sativa Predicted polypeptide sequence is paralogous to G3652,G3653, G3654; orthologous to G2576, G872 804 G3655 PRT Oryza sativaParalogous to G3652, G3653, G3654; orthologous to G2576, G872 805 G3656DNA Zea mays Predicted polypeptide sequence is orthologous to G12,G1277, G1379, G24 806 G3656 PRT Zea mays Orthologous to G12, G1277,G1379, G24 Os_S32369 DNA Oryza sativa Predicted polypeptide sequence isorthologous to G24 Os_S80194 DNA Oryza sativa Predicted polypeptidesequence is orthologous to G24 Os_S60918 DNA Oryza sativa Predictedpolypeptide sequence is orthologous to G154 Os_S112966 DNA Oryza sativaPredicted polypeptide sequence is orthologous to G384 Os_S113503 DNAOryza sativa Predicted polypeptide sequence is orthologous to G384Os_S96499 DNA Oryza sativa Predicted polypeptide sequence is orthologousto G1868 Os_S60490 DNA Oryza sativa Predicted polypeptide sequence isorthologous to G1888 Os_S60479 DNA Oryza sativa Predicted polypeptidesequence is orthologous to G200 Os_S100515 DNA Oryza sativa Predictedpolypeptide sequence is orthologous to G347 Os_S60901 DNA Oryza sativaPredicted polypeptide sequence is orthologous to G427 Os_S64872 DNAOryza sativa Predicted polypeptide sequence is orthologous to G427Os_S64899 DNA Oryza sativa Predicted polypeptide sequence is orthologousto G427 Os_S64900 DNA Oryza sativa Predicted polypeptide sequence isorthologous to G427 Os_S113396 DNA Oryza sativa Predicted polypeptidesequence is orthologous to G618, G2057 Os_S113398 DNA Oryza sativaPredicted polypeptide sequence is orthologous to G618, G2057 Os_S76089DNA Oryza sativa Predicted polypeptide sequence is orthologous to G653Os_S44434 DNA Oryza sativa Predicted polypeptide sequence is orthologousto G866 Os_S116938 DNA Oryza sativa Predicted polypeptide sequence isorthologous to G912 Os_S116940 DNA Oryza sativa Predicted polypeptidesequence is orthologous to G912 Os_S117813 DNA Oryza sativa Predictedpolypeptide sequence is orthologous to G912 Os_S65912 DNA Oryza sativaPredicted polypeptide sequence is orthologous to G912 Os_S61189 DNAOryza sativa Predicted polypeptide sequence is orthologous to G958Os_S69951 DNA Oryza sativa Predicted polypeptide sequence is orthologousto G958 Os_S98061 DNA Oryza sativa Predicted polypeptide sequence isorthologous to G1535 Os_S75175 DNA Oryza sativa Predicted polypeptidesequence is orthologous to G1930 Gma_S5071803 DNA Glycine max Predictedpolypeptide sequence is orthologous to G24 Gma_S5094568 DNA Glycine maxPredicted polypeptide sequence is orthologous to G154 Gma_S4992142 DNAGlycine max Predicted polypeptide sequence is orthologous to G384Gma_S4873409 DNA Glycine max Predicted polypeptide sequence isorthologous to G545 Gma_S5146663 DNA Glycine max Predicted polypeptidesequence is orthologous to G545 Gma_S4883349 DNA Glycine max Predictedpolypeptide sequence is orthologous to G760 Gma_S5050636 DNA Glycine maxPredicted polypeptide sequence is orthologous to G773 Gma_S5129137 DNAGlycine max Predicted polypeptide sequence is orthologous to G937Gma_S4904682 DNA Glycine max Predicted polypeptide sequence isorthologous to G1322 Gma_S5045510 DNA Glycine max Predicted polypeptidesequence is orthologous to G2520 Gma_S4864518 DNA Glycine max Predictedpolypeptide sequence is orthologous to G2522 Gma_S4935598 DNA Glycinemax Predicted polypeptide sequence is orthologous to G2789 Gma_S4901804DNA Glycine max Predicted polypeptide sequence is orthologous to G189Gma_S4898629 DNA Glycine max Predicted polypeptide sequence isorthologous to G275, G837 Gma_S4907362 DNA Glycine max Predictedpolypeptide sequence is orthologous to G275, G837 Gma_S4934838 DNAGlycine max Predicted polypeptide sequence is orthologous to G347Gma_S4867945 DNA Glycine max Predicted polypeptide sequence isorthologous to G427 Gma_S4863794 DNA Glycine max Predicted polypeptidesequence is orthologous to G602 Gma_S5029115 DNA Glycine max Predictedpolypeptide sequence is orthologous to G618, G2057 Gma_S4874203 DNAGlycine max Predicted polypeptide sequence is orthologous to G866Gma_S4886425 DNA Glycine max Predicted polypeptide sequence isorthologous to G866 Gma_S5106568 DNA Glycine max Predicted polypeptidesequence is orthologous to G866 Gma_S5001940 DNA Glycine max Predictedpolypeptide sequence is orthologous to G964 Gma_S5131758 DNA Glycine maxPredicted polypeptide sequence is orthologous to G1049 Gma_S4889036 DNAGlycine max Predicted polypeptide sequence is orthologous to G1835Gma_S4911179 DNA Glycine max Predicted polypeptide sequence isorthologous to G1835 Gma_S5137324 DNA Glycine max Predicted polypeptidesequence is orthologous to G2535 Mtr_S5349908 DNA Medicago truncatulaPredicted polypeptide sequence is orthologous to G24 Mtr_S5357829 DNAMedicago truncatula Predicted polypeptide sequence is orthologous toG154 Mtr_S5447672 DNA Medicago truncatula Predicted polypeptide sequenceis orthologous to G384 Mtr_S5317695 DNA Medicago truncatula Predictedpolypeptide sequence is orthologous to G545 Mtr_S5431156 DNA Medicagotruncatula Predicted polypeptide sequence is orthologous to G545Mtr_S5340844 DNA Medicago truncatula Predicted polypeptide sequence isorthologous to G760 Mtr_S7090764 DNA Medicago truncatula Predictedpolypeptide sequence is orthologous to G760 Mtr_S10820905 DNA Medicagotruncatula Predicted polypeptide sequence is orthologous to G1888Mtr_S10821012 DNA Medicago truncatula Predicted polypeptide sequence isorthologous to G275, G837 Mtr_S5454462 DNA Medicago truncatula Predictedpolypeptide sequence is orthologous to G347 Mtr_S5306926 DNA Medicagotruncatula Predicted polypeptide sequence is orthologous to G427Mtr_S5449876 DNA Medicago truncatula Predicted polypeptide sequence isorthologous to G427 Mtr_S7092065 DNA Medicago truncatula Predictedpolypeptide sequence is orthologous to G427 Mtr_S5431439 DNA Medicagotruncatula Predicted polypeptide sequence is orthologous to G602Mtr_S5399163 DNA Medicago truncatula Predicted polypeptide sequence isorthologous to G635 Mtr_S7091176 DNA Medicago truncatula Predictedpolypeptide sequence is orthologous to G653 Mtr_S5305224 DNA Medicagotruncatula Predicted polypeptide sequence is orthologous to G866Mtr_S7091692 DNA Medicago truncatula Predicted polypeptide sequence isorthologous to G866 Mtr_S5409553 DNA Medicago truncatula Predictedpolypeptide sequence is orthologous to G1255 Mtr_S5430627 DNA Medicagotruncatula Predicted polypeptide sequence is orthologous to G1930Hv_S30279 DNA Hordeum vulgare Predicted polypeptide sequence isorthologous to G384 Hv_S36040 DNA Hordeum vulgare Predicted polypeptidesequence is orthologous to G2522 Hv_S8292 DNA Hordeum vulgare Predictedpolypeptide sequence is orthologous to G275, G837 Hv_S67575 DNA Hordeumvulgare Predicted polypeptide sequence is orthologous to G326 Hv_S23303DNA Hordeum vulgare Predicted polypeptide sequence is orthologous toG427 Hv_S136844 DNA Hordeum vulgare Predicted polypeptide sequence isorthologous to G653 Hv_S152300 DNA Hordeum vulgare Predicted polypeptidesequence is orthologous to G912 Hv_S158942 DNA Hordeum vulgare Predictedpolypeptide sequence is orthologous to G912 Hv_S74288 DNA Hordeumvulgare Predicted polypeptide sequence is orthologous to G912 Hv_S74289DNA Hordeum vulgare Predicted polypeptide sequence is orthologous toG912 Hv_S20601 DNA Hordeum vulgare Predicted polypeptide sequence isorthologous to G2512 Zm_S11418746 DNA Zea mays Predicted polypeptidesequence is orthologous to G154 Zm_S11527819 DNA Zea mays Predictedpolypeptide sequence is orthologous to G154 Zm_S11333633 DNA Zea maysPredicted polypeptide sequence is orthologous to G384 Zm_S11401894 DNAZea mays Predicted polypeptide sequence is orthologous to G384Zm_S11418286 DNA Zea mays Predicted polypeptide sequence is orthologousto G384 Zm_S11418453 DNA Zea mays Predicted polypeptide sequence isorthologous to G384 Zm_S11418455 DNA Zea mays Predicted polypeptidesequence is orthologous to G384 Zm_S11523949 DNA Zea mays Predictedpolypeptide sequence is orthologous to G384 Zm_S11441492 DNA Zea maysPredicted polypeptide sequence is orthologous to G545 Zm_S11443346 DNAZea mays Predicted polypeptide sequence is orthologous to G545Zm_S11465527 DNA Zea mays Predicted polypeptide sequence is orthologousto G545 Zm_S11526816 DNA Zea mays Predicted polypeptide sequence isorthologous to G760 Zm_S11529038 DNA Zea mays Predicted polypeptidesequence is orthologous to G760 Zm_S11529147 DNA Zea mays Predictedpolypeptide sequence is orthologous to G1322 Zm_S11522646 DNA Zea maysPredicted polypeptide sequence is orthologous to G1868 Zm_S11522707 DNAZea mays Predicted polypeptide sequence is orthologous to G1868Zm_S11525236 DNA Zea mays Predicted polypeptide sequence is orthologousto G1868 Zm_S11432778 DNA Zea mays Predicted polypeptide sequence isorthologous to G1888 Zm_S11528772 DNA Zea mays Predicted polypeptidesequence is orthologous to G2131, G979 Zm_S11524369 DNA Zea maysPredicted polypeptide sequence is orthologous to G2520 Zm_S11529138 DNAZea mays Predicted polypeptide sequence is orthologous to G200Zm_S11529143 DNA Zea mays Predicted polypeptide sequence is orthologousto G200 Zm_S11529165 DNA Zea mays Predicted polypeptide sequence isorthologous to G200 Zm_S11529159 DNA Zea mays Predicted polypeptidesequence is orthologous to G234 Zm_S11529194 DNA Zea mays Predictedpolypeptide sequence is orthologous to G234 Zm_S11528144 DNA Zea maysPredicted polypeptide sequence is orthologous to G275, G837 Zm_S11450524DNA Zea mays Predicted polypeptide sequence is orthologous to G326Zm_S11510508 DNA Zea mays Predicted polypeptide sequence is orthologousto G326 Zm_S11437336 DNA Zea mays Predicted polypeptide sequence isorthologous to G347 Zm_S11520104 DNA Zea mays Predicted polypeptidesequence is orthologous to G347 Zm_S11442066 DNA Zea mays Predictedpolypeptide sequence is orthologous to G427 Zm_S11452342 DNA Zea maysPredicted polypeptide sequence is orthologous to G427 Zm_S11527509 DNAZea mays Predicted polypeptide sequence is orthologous to G427Zm_S11527752 DNA Zea mays Predicted polypeptide sequence is orthologousto G602 Zm_S11528938 DNA Zea mays Predicted polypeptide sequence isorthologous to G653 Zm_S11523935 DNA Zea mays Predicted polypeptidesequence is orthologous to G866 Zm_S11519368 DNA Zea mays Predictedpolypeptide sequence is orthologous to G912 Zm_S11524655 DNA Zea maysPredicted polypeptide sequence is orthologous to G932 Zm_S11529150 DNAZea mays Predicted polypeptide sequence is orthologous to G932Zm_S11529161 DNA Zea mays Predicted polypeptide sequence is orthologousto G932 Zm_S11529174 DNA Zea mays Predicted polypeptide sequence isorthologous to G932 Zm_S11529193 DNA Zea mays Predicted polypeptidesequence is orthologous to G932 Zm_S11437468 DNA Zea mays Predictedpolypeptide sequence is orthologous to G958 Zm_S11445843 DNA Zea maysPredicted polypeptide sequence is orthologous to G1049 Zm_S11485770 DNAZea mays Predicted polypeptide sequence is orthologous to G1255Zm_S11529198 DNA Zea mays Predicted polypeptide sequence is orthologousto G1331 Zm_S11418454 DNA Zea mays Predicted polypeptide sequence isorthologous to G1535 Zm_S11522858 DNA Zea mays Predicted polypeptidesequence is orthologous to G1535 Zm_S11506592 DNA Zea mays Predictedpolypeptide sequence is orthologous to G1930 Ta_S203038 DNA Triticumaestivum Predicted polypeptide sequence is orthologous to G154Ta_S424724 DNA Triticum aestivum Predicted polypeptide sequence isorthologous to G154 Ta_S133393 DNA Triticum aestivum Predictedpolypeptide sequence is orthologous to G384 Ta_S147812 DNA Triticumaestivum Predicted polypeptide sequence is orthologous to G545 Ta_S66284DNA Triticum aestivum Predicted polypeptide sequence is orthologous toG545 Ta_S202572 DNA Triticum aestivum Predicted polypeptide sequence isorthologous to G760 Ta_S178842 DNA Triticum aestivum Predictedpolypeptide sequence is orthologous to G1868 Ta_S84222 DNA Triticumaestivum Predicted polypeptide sequence is orthologous to G2520Ta_S115031 DNA Triticum aestivum Predicted polypeptide sequence isorthologous to G2522 Ta_S65435 DNA Triticum aestivum Predictedpolypeptide sequence is orthologous to G2522 Ta_S177690 DNA Triticumaestivum Predicted polypeptide sequence is orthologous to G8 Ta_S148486DNA Triticum aestivum Predicted polypeptide sequence is orthologous toG326 Ta_S64707 DNA Triticum aestivum Predicted polypeptide sequence isorthologous to G347 Ta_S16327 DNA Triticum aestivum Predictedpolypeptide sequence is orthologous to G427 Ta_S201090 DNA Triticumaestivum Predicted polypeptide sequence is orthologous to G427 Ta_S2764DNA Triticum aestivum Predicted polypeptide sequence is orthologous toG635 Ta_S166473 DNA Triticum aestivum Predicted polypeptide sequence isorthologous to G653 Ta_S174179 DNA Triticum aestivum Predictedpolypeptide sequence is orthologous to G866 Ta_S280279 DNA Triticumaestivum Predicted polypeptide sequence is orthologous to G866 Ta_S47586DNA Triticum aestivum Predicted polypeptide sequence is orthologous toG912 Ta_S75229 DNA Triticum aestivum Predicted polypeptide sequence isorthologous to G912 Ta_S203158 DNA Triticum aestivum Predictedpolypeptide sequence is orthologous to G1255 Ta_S363550 DNA Triticumaestivum Predicted polypeptide sequence is orthologous to G1255Ta_S142289 DNA Triticum aestivum Predicted polypeptide sequence isorthologous to G1835 Ta_S266353 DNA Triticum aestivum Predictedpolypeptide sequence is orthologous to G1835 Ta_S174040 DNA Triticumaestivum Predicted polypeptide sequence is orthologous to G2145Les_S5295933 DNA Lycopersicon Predicted polypeptide sequence isesculentum orthologous to G154 Les_S5295623 DNA Lycopersicon Predictedpolypeptide sequence is esculentum orthologous to G773 Les_S5295726 DNALycopersicon Predicted polypeptide sequence is esculentum orthologous toG988 Les_S5183164 DNA Lycopersicon Predicted polypeptide sequence isesculentum orthologous to G2520 Les_S5203454 DNA Lycopersicon Predictedpolypeptide sequence is esculentum orthologous to G2520 Les_S6657758 DNALycopersicon Predicted polypeptide sequence is esculentum orthologous toG189 Les_S5275585 DNA Lycopersicon Predicted polypeptide sequence isesculentum orthologous to G347 Les_S5295728 DNA Lycopersicon Predictedpolypeptide sequence is esculentum orthologous to G427 Les_S5295749 DNALycopersicon Predicted polypeptide sequence is esculentum orthologous toG427 Les_S5295478 DNA Lycopersicon Predicted polypeptide sequence isesculentum orthologous to G618, G2057 Les_S6657761 DNA LycopersiconPredicted polypeptide sequence is esculentum orthologous to G866Les_S6657762 DNA Lycopersicon Predicted polypeptide sequence isesculentum orthologous to G866 Les_S5295301 DNA Lycopersicon Predictedpolypeptide sequence is esculentum orthologous to G912 Les_S5295595 DNALycopersicon Predicted polypeptide sequence is esculentum orthologous toG932 Les_S5269007 DNA Lycopersicon Predicted polypeptide sequence isesculentum orthologous to G1266 Les_S5295266 DNA Lycopersicon Predictedpolypeptide sequence is esculentum orthologous to G1266 Les_S5295755 DNALycopersicon Predicted polypeptide sequence is esculentum orthologous toG1266 Les_S6682822 DNA Lycopersicon Predicted polypeptide sequence isesculentum orthologous to G1266 Les_S5295754 DNA Lycopersicon Predictedpolypeptide sequence is esculentum orthologous to G1750 SGN- DNALycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G24 49683 SGN- DNA Lycopersicon Predicted polypeptidesequence is UNIGENE- esculentum orthologous to G24 54594 SGN- DNALycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G24 SINGLET-47313 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G154 50586SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G154 52410 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G154 SINGLET-366830 SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G154 SINGLET- 394847 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG384 SINGLET-17776 SGN- DNA Lycopersicon Predicted polypeptide sequenceis UNIGENE- esculentum orthologous to G545 44163 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG545 44287 SGN- DNA Lycopersicon Predicted polypeptide sequence isUNIGENE- esculentum orthologous to G545 SINGLET-6983 SGN- DNALycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G760 47781 SGN- DNA Lycopersicon Predicted polypeptidesequence is UNIGENE- esculentum orthologous to G760 52634 SGN- DNALycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G760 53754 SGN- DNA Lycopersicon Predicted polypeptidesequence is UNIGENE- esculentum orthologous to G760 SINGLET-23750 SGN-DNA Lycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G760 SINGLET- 310313 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G760 SINGLET-447414 SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G773 45948 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G773 48215SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G1069 59076 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G1090 54402SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G1322 58620 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G1322SINGLET-16950 SGN- DNA Lycopersicon Predicted polypeptide sequence isUNIGENE- esculentum orthologous to G1868 48848 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG1868 SINGLET- 453383 SGN- DNA Lycopersicon Predicted polypeptidesequence is UNIGENE- esculentum orthologous to G1888 47593 SGN- DNALycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G2131, G979 SINGLET-517 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G2520 44928SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G2522 50326 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G8 SINGLET-395477 SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G156 54690 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G161 57990SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G200 57276 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G200 SINGLET-385670 SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G234 SINGLET-21166 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG275, G837 47489 SGN- DNA Lycopersicon Predicted polypeptide sequence isUNIGENE- esculentum orthologous to G275, G837 47510 SGN- DNALycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G275, G837 51256 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G275, G83756050 SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G326 SINGLET-19083 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG347 51747 SGN- DNA Lycopersicon Predicted polypeptide sequence isUNIGENE- esculentum orthologous to G427 51523 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG427 54900 SGN- DNA Lycopersicon Predicted polypeptide sequence isUNIGENE- esculentum orthologous to G427 55550 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG427 55551 SGN- DNA Lycopersicon Predicted polypeptide sequence isUNIGENE- esculentum orthologous to G427 SINGLET- 397654 SGN- DNALycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G427 SINGLET- 446384 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G427SINGLET-50339 SGN- DNA Lycopersicon Predicted polypeptide sequence isUNIGENE- esculentum orthologous to G427 SINGLET-9520 SGN- DNALycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G590 47483 SGN- DNA Lycopersicon Predicted polypeptidesequence is UNIGENE- esculentum orthologous to G590 47925 SGN- DNALycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G602 SINGLET-2565 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G618, G205750577 SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G618, G2057 58580 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG618, G2057 SINGLET-24189 SGN- DNA Lycopersicon Predicted polypeptidesequence is UNIGENE- esculentum orthologous to G618, G2057 SINGLET-394109 SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G618, G2057 SINGLET- 401522 SGN- DNALycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G643 56459 SGN- DNA Lycopersicon Predicted polypeptidesequence is UNIGENE- esculentum orthologous to G653 46400 SGN- DNALycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G653 SINGLET-64524 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G866 45903SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G866 SINGLET- 439904 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG872 50296 SGN- DNA Lycopersicon Predicted polypeptide sequence isUNIGENE- esculentum orthologous to G912 46974 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG912 46975 SGN- DNA Lycopersicon Predicted polypeptide sequence isUNIGENE- esculentum orthologous to G912 58571 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG912 SINGLET- 398604 SGN- DNA Lycopersicon Predicted polypeptidesequence is UNIGENE- esculentum orthologous to G932 52504 SGN- DNALycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G932 52540 SGN- DNA Lycopersicon Predicted polypeptidesequence is UNIGENE- esculentum orthologous to G932 57232 SGN- DNALycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G975 SINGLET-14957 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G975 SINGLET-335836 SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G1049 SINGLET- 333614 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG1255 48698 SGN- DNA Lycopersicon Predicted polypeptide sequence isUNIGENE- esculentum orthologous to G1255 53476 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG1255 54828 SGN- DNA Lycopersicon Predicted polypeptide sequence isUNIGENE- esculentum orthologous to G1266 48067 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG1266 49923 SGN- DNA Lycopersicon Predicted polypeptide sequence isUNIGENE- esculentum orthologous to G1266 52630 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG1266 SINGLET-38956 SGN- DNA Lycopersicon Predicted polypeptide sequenceis UNIGENE- esculentum orthologous to G1535 SINGLET-13754 SGN- DNALycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G1750 49801 SGN- DNA Lycopersicon Predicted polypeptidesequence is UNIGENE- esculentum orthologous to G1750 SINGLET-2078 SGN-DNA Lycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G1750 SINGLET- 446513 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G1835 48476SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G1835 51325 SGN- DNA Lycopersicon Predictedpolypeptide sequence is UNIGENE- esculentum orthologous to G1930 47598SGN- DNA Lycopersicon Predicted polypeptide sequence is UNIGENE-esculentum orthologous to G1930 SINGLET- 393621 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG1930 SINGLET-44327 SGN- DNA Lycopersicon Predicted polypeptide sequenceis UNIGENE- esculentum orthologous to G2144 51335 SGN- DNA LycopersiconPredicted polypeptide sequence is UNIGENE- esculentum orthologous toG2512 SINGLET-2865 SGN- DNA Lycopersicon Predicted polypeptide sequenceis UNIGENE- esculentum orthologous to G2535 SINGLET- 366637 SGN- DNALycopersicon Predicted polypeptide sequence is UNIGENE- esculentumorthologous to G2719 SINGLET- 357168 Vvi_S15370190 DNA Vitis viniferaPredicted polypeptide sequence is orthologous to G24 Vvi_S16806812 DNAVitis vinifera Predicted polypeptide sequence is orthologous to G24Vvi_S15373999 DNA Vitis vinifera Predicted polypeptide sequence isorthologous to G154 Vvi_S16872184 DNA Vitis vinifera Predictedpolypeptide sequence is orthologous to G154 Vvi_S15355617 DNA Vitisvinifera Predicted polypeptide sequence is orthologous to G545Vvi_S15382170 DNA Vitis vinifera Predicted polypeptide sequence isorthologous to G545 Vvi_S16873427 DNA Vitis vinifera Predictedpolypeptide sequence is orthologous to G760 Vvi_S15431951 DNA Vitisvinifera Predicted polypeptide sequence is orthologous to G937Vvi_S16805106 DNA Vitis vinifera Predicted polypeptide sequence isorthologous to G937 Vvi_S16805621 DNA Vitis vinifera Predictedpolypeptide sequence is orthologous to G1069 Vvi_S15388842 DNA Vitisvinifera Predicted polypeptide sequence is orthologous to G1322Vvi_S15421316 DNA Vitis vinifera Predicted polypeptide sequence isorthologous to G2520 Vvi_S16529182 DNA Vitis vinifera Predictedpolypeptide sequence is orthologous to G2520 Vvi_S15370801 DNA Vitisvinifera Predicted polypeptide sequence is orthologous to G2522Vvi_S15411435 DNA Vitis vinifera Predicted polypeptide sequence isorthologous to G8 Vvi_S15353287 DNA Vitis vinifera Predicted polypeptidesequence is orthologous to G189 Vvi_S15374453 DNA Vitis viniferaPredicted polypeptide sequence is orthologous to G189 Vvi_S15426449 DNAVitis vinifera Predicted polypeptide sequence is orthologous to G275,G837 Vvi_S16870363 DNA Vitis vinifera Predicted polypeptide sequence isorthologous to G275, G837 Vvi_S16531517 DNA Vitis vinifera Predictedpolypeptide sequence is orthologous to G347 Vvi_S15401282 DNA Vitisvinifera Predicted polypeptide sequence is orthologous to G427Vvi_S15423741 DNA Vitis vinifera Predicted polypeptide sequence isorthologous to G427 Vvi_S15353882 DNA Vitis vinifera Predictedpolypeptide sequence is orthologous to G602 Vvi_S15426604 DNA Vitisvinifera Predicted polypeptide sequence is orthologous to G653Vvi_S15374416 DNA Vitis vinifera Predicted polypeptide sequence isorthologous to G866 Vvi_S16870232 DNA Vitis vinifera Predictedpolypeptide sequence is orthologous to G872 Vvi_S15357313 DNA Vitisvinifera Predicted polypeptide sequence is orthologous to G912Vvi_S15391707 DNA Vitis vinifera Predicted polypeptide sequence isorthologous to G912 Vvi_S16532074 DNA Vitis vinifera Predictedpolypeptide sequence is orthologous to G932 Vvi_S15427527 DNA Vitisvinifera Predicted polypeptide sequence is orthologous to G1255Vvi_S15431583 DNA Vitis vinifera Predicted polypeptide sequence isorthologous to G1255 Vvi_S16871195 DNA Vitis vinifera Predictedpolypeptide sequence is orthologous to G1494 Vvi_S16865934 DNA Vitisvinifera Predicted polypeptide sequence is orthologous to G1835Vvi_S16529913 DNA Vitis vinifera Predicted polypeptide sequence isorthologous to G2144 Pta_S15732813 DNA Pinus taeda Predicted polypeptidesequence is orthologous to G154 Pta_S15736271 DNA Pinus taeda Predictedpolypeptide sequence is orthologous to G154 Pta_S15739572 DNA Pinustaeda Predicted polypeptide sequence is orthologous to G154Pta_S15740527 DNA Pinus taeda Predicted polypeptide sequence isorthologous to G154 Pta_S15746398 DNA Pinus taeda Predicted polypeptidesequence is orthologous to G154 Pta_S15751737 DNA Pinus taeda Predictedpolypeptide sequence is orthologous to G154 Pta_S15777399 DNA Pinustaeda Predicted polypeptide sequence is orthologous to G154Pta_S15780122 DNA Pinus taeda Predicted polypeptide sequence isorthologous to G154 Pta_S15795745 DNA Pinus taeda Predicted polypeptidesequence is orthologous to G154 Pta_S16849782 DNA Pinus taeda Predictedpolypeptide sequence is orthologous to G154 Pta_S16789085 DNA Pinustaeda Predicted polypeptide sequence is orthologous to G760Pta_S17046663 DNA Pinus taeda Predicted polypeptide sequence isorthologous to G1666 Pta_S16800293 DNA Pinus taeda Predicted polypeptidesequence is orthologous to G1868 Pta_S15767209 DNA Pinus taeda Predictedpolypeptide sequence is orthologous to G2522 Pta_S15799222 DNA Pinustaeda Predicted polypeptide sequence is orthologous to G2789Pta_S16786360 DNA Pinus taeda Predicted polypeptide sequence isorthologous to G2789 Pta_S16788492 DNA Pinus taeda Predicted polypeptidesequence is orthologous to G2789 Pta_S16802054 DNA Pinus taeda Predictedpolypeptide sequence is orthologous to G2789 Pta_S16793418 DNA Pinustaeda Predicted polypeptide sequence is orthologous to G189Pta_S15736214 DNA Pinus taeda Predicted polypeptide sequence isorthologous to G275, G837 Pta_S15776645 DNA Pinus taeda Predictedpolypeptide sequence is orthologous to G275, G837 Pta_S17049915 DNAPinus taeda Predicted polypeptide sequence is orthologous to G326Pta_S16847381 DNA Pinus taeda Predicted polypeptide sequence isorthologous to G427 Pta_S17051722 DNA Pinus taeda Predicted polypeptidesequence is orthologous to G427 Pta_S16797626 DNA Pinus taeda Predictedpolypeptide sequence is orthologous to G602 Pta_S16790444 DNA Pinustaeda Predicted polypeptide sequence is orthologous to G653Pta_S17050802 DNA Pinus taeda Predicted polypeptide sequence isorthologous to G653 Pta_S15754706 DNA Pinus taeda Predicted polypeptidesequence is orthologous to G872 Pta_S15767728 DNA Pinus taeda Predictedpolypeptide sequence is orthologous to G872 Pta_S15779272 DNA Pinustaeda Predicted polypeptide sequence is orthologous to G872Pta_S15738910 DNA Pinus taeda Predicted polypeptide sequence isorthologous to G958 Pta_S15774939 DNA Pinus taeda Predicted polypeptidesequence is orthologous to G958 Pta_S15797996 DNA Pinus taeda Predictedpolypeptide sequence is orthologous to G964 807 G1048 DNA Arabidopsisthaliana 808 G1048 PRT Arabidopsis thaliana 809 G1100 DNA Arabidopsisthaliana 810 G1100 PRT Arabidopsis thaliana 811 G1796 DNA Arabidopsisthaliana 812 G1796 PRT Arabidopsis thaliana 813 G1995 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2826, G2838,G361, G362, G370 814 G1995 PRT Arabidopsis thaliana Paralogous to G2826,G2838, G361, G362, G370 815 G2467 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G812 816 G2467 PRT Arabidopsisthaliana Paralogous to G812 817 G2505 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G2635 818 G2505 PRT Arabidopsisthaliana Paralogous to G2635 819 G2550 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G2546 820 G2550 PRTArabidopsis thaliana Paralogous to G2546 821 G2640 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2639, G2642822 G2640 PRT Arabidopsis thaliana Paralogous to G2639, G2642 823 G2686DNA Arabidopsis thaliana Predicted polypeptide sequence is paralogous toG2586, G2587 824 G2686 PRT Arabidopsis thaliana Paralogous to G2586,G2587 825 G38 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G1141 826 G38 PRT Arabidopsis thaliana Paralogous to G1141827 G44 DNA Arabidopsis thaliana 828 G44 PRT Arabidopsis thaliana 829G230 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G207, G227, G242 830 G230 PRT Arabidopsis thalianaParalogous to G207, G227, G242 831 G261 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G265 832 G261 PRTArabidopsis thaliana Paralogous to G265 833 G271 DNA Arabidopsisthaliana 834 G271 PRT Arabidopsis thaliana 835 G359 DNA Arabidopsisthaliana 836 G359 PRT Arabidopsis thaliana 837 G377 DNA Arabidopsisthaliana 838 G377 PRT Arabidopsis thaliana 839 G388 DNA Arabidopsisthaliana 840 G388 PRT Arabidopsis thaliana 841 G435 DNA Arabidopsisthaliana 842 G435 PRT Arabidopsis thaliana 843 G442 DNA Arabidopsisthaliana 844 G442 PRT Arabidopsis thaliana 845 G468 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G2866 846 G468PRT Arabidopsis thaliana Paralogous to G2866 847 G571 DNA Arabidopsisthaliana 848 G571 PRT Arabidopsis thaliana 849 G652 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G1335 850 G652PRT Arabidopsis thaliana Paralogous to G1335 851 G664 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G197, G255;orthologous to G3503, G3504, G3505, G3506, G3507, G3508, G3509, G3529,G3531, G3532, G3533, G3534, G3527, G3528 852 G664 PRT Arabidopsisthaliana Paralogous to G197, G255; Orthologous to G3503, G3504, G3505,G3506, G3507, G3508, G3509, G3529, G3531, G3532, G3533, G3534, G3527,G3528 853 G772 DNA Arabidopsis thaliana Predicted polypeptide sequenceis paralogous to G776 854 G772 PRT Arabidopsis thaliana Paralogous toG776 855 G798 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G1897 856 G798 PRT Arabidopsis thaliana Paralogous toG1897 857 G818 DNA Arabidopsis thaliana 858 G818 PRT Arabidopsisthaliana 859 G974 DNA Arabidopsis thaliana Predicted polypeptidesequence is paralogous to G5 860 G974 PRT Arabidopsis thalianaParalogous to G5 861 G1062 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G1664 862 G1062 PRT Arabidopsisthaliana Paralogous to G1664 863 G1129 DNA Arabidopsis thaliana 864G1129 PRT Arabidopsis thaliana 865 G1137 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G1133 866 G1137 PRTArabidopsis thaliana Paralogous to G1133 867 G1425 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G1454, G504;orthologous to G3809 868 G1425 PRT Arabidopsis thaliana Paralogous toG1454, G504; Orthologous to G3809 869 G1517 DNA Arabidopsis thaliana 870G1517 PRT Arabidopsis thaliana 871 G1655 DNA Arabidopsis thaliana 872G1655 PRT Arabidopsis thaliana 873 G1743 DNA Arabidopsis thaliana 874G1743 PRT Arabidopsis thaliana 875 G1789 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G1911, G2721, G997 876G1789 PRT Arabidopsis thaliana Paralogous to G1911, G2721, G997 877G1806 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G1198, G554, G555, G556, G558, G578, G629 878 G1806 PRTArabidopsis thaliana Paralogous to G1198, G554, G555, G556, G558, G578,G629 879 G1911 DNA Arabidopsis thaliana Predicted polypeptide sequenceis paralogous to G1789, G2721, G997 880 G1911 PRT Arabidopsis thalianaParalogous to G1789, G2721, G997 881 G2011 DNA Arabidopsis thaliana 882G2011 PRT Arabidopsis thaliana 883 G2215 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G2216 884 G2215 PRTArabidopsis thaliana Paralogous to G2216 885 G2452 DNA Arabidopsisthaliana 886 G2452 PRT Arabidopsis thaliana 887 G2455 DNA Arabidopsisthaliana 888 G2455 PRT Arabidopsis thaliana 889 G2510 DNA Arabidopsisthaliana 890 G2510 PRT Arabidopsis thaliana 891 G2515 DNA Arabidopsisthaliana 892 G2515 PRT Arabidopsis thaliana 893 G2571 DNA Arabidopsisthaliana 894 G2571 PRT Arabidopsis thaliana 895 G2702 DNA Arabidopsisthaliana 896 G2702 PRT Arabidopsis thaliana 897 G2763 DNA Arabidopsisthaliana 898 G2763 PRT Arabidopsis thaliana 899 G2774 DNA Arabidopsisthaliana 900 G2774 PRT Arabidopsis thaliana 901 G2888 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G1991 902 G2888PRT Arabidopsis thaliana Paralogous to G1991 903 G2958 DNA Arabidopsisthaliana 904 G2958 PRT Arabidopsis thaliana 905 G5 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G974 906 G5 PRTArabidopsis thaliana Paralogous to G974 907 G197 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G255, G664;orthologous to G3503, G3504, G3505, G3506, G3507, G3508, G3509, G3529,G3531, G3532, G3533, G3534, G3527, G3528 908 G197 PRT Arabidopsisthaliana Paralogous to G255, G664; Orthologous to G3503, G3504, G3505,G3506, G3507, G3508, G3509, G3529, G3531, G3532, G3533, G3534, G3527,G3528 909 G207 DNA Arabidopsis thaliana Predicted polypeptide sequenceis paralogous to G227, G230, G242 910 G207 PRT Arabidopsis thalianaParalogous to G227, G230, G242 911 G227 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G207, G230, G242 912G227 PRT Arabidopsis thaliana Paralogous to G207, G230, G242 913 G242DNA Arabidopsis thaliana Predicted polypeptide sequence is paralogous toG207, G227, G230 914 G242 PRT Arabidopsis thaliana Paralogous to G207,G227, G230 915 G255 DNA Arabidopsis thaliana Predicted polypeptidesequence is paralogous to G197, G664; orthologous to G3503, G3504,G3505, G3506, G3507, G3508, G3509, G3529, G3531, G3532, G3533, G3534,G3527, G3528 916 G255 PRT Arabidopsis thaliana Paralogous to G197, G664;Orthologous to G3503, G3504, G3505, G3506, G3507, G3508, G3509, G3529,G3531, G3532, G3533, G3534, G3527, G3528 917 G265 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G261 918 G265PRT Arabidopsis thaliana Paralogous to G261 919 G361 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G1995, G2826,G2838, G362, G370 920 G361 PRT Arabidopsis thaliana Paralogous to G1995,G2826, G2838, G362, G370 921 G362 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G1995, G2826, G2838, G361, G370922 G362 PRT Arabidopsis thaliana Paralogous to G1995, G2826, G2838,G361, G370 923 G370 DNA Arabidopsis thaliana Predicted polypeptidesequence is paralogous to G1995, G2826, G2838, G361, G362 924 G370 PRTArabidopsis thaliana Paralogous to G1995, G2826, G2838, G361, G362 925G504 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G1425, G1454; orthologous to G3809 926 G504 PRTArabidopsis thaliana Paralogous to G1425, G1454; Orthologous to G3809927 G554 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G1198, G1806, G555, G556, G558, G578, G629 928 G554 PRTArabidopsis thaliana Paralogous to G1198, G1806, G555, G556, G558, G578,G629 929 G555 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G1198, G1806, G554, G556, G558, G578, G629 930 G555 PRTArabidopsis thaliana Paralogous to G1198, G1806, G554, G556, G558, G578,G629 931 G556 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G1198, G1806, G554, G555, G558, G578, G629 932 G556 PRTArabidopsis thaliana Paralogous to G1198, G1806, G554, G555, G558, G578,G629 933 G558 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G1198, G1806, G554, G555, G556, G578, G629 934 G558 PRTArabidopsis thaliana Paralogous to G1198, G1806, G554, G555, G556, G578,G629 935 G578 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G1198, G1806, G554, G555, G556, G558, G629 936 G578 PRTArabidopsis thaliana Paralogous to G1198, G1806, G554, G555, G556, G558,G629 937 G629 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G1198, G1806, G554, G555, G556, G558, G578 938 G629 PRTArabidopsis thaliana Paralogous to G1198, G1806, G554, G555, G556, G558,G578 939 G776 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G772 940 G776 PRT Arabidopsis thaliana Paralogous to G772941 G812 DNA Arabidopsis thaliana Predicted polypeptide sequence isparalogous to G2467 942 G812 PRT Arabidopsis thaliana Paralogous toG2467 943 G997 DNA Arabidopsis thaliana Predicted polypeptide sequenceis paralogous to G1789, G1911, G2721 944 G997 PRT Arabidopsis thalianaParalogous to G1789, G1911, G2721 945 G1133 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G1137 946 G1133 PRTArabidopsis thaliana Paralogous to G1137 947 G1141 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G38 948 G1141PRT Arabidopsis thaliana Paralogous to G38 949 G1198 DNA Arabidopsisthaliana Predicted polypeptide sequence is paralogous to G1806, G554,G555, G556, G558, G578, G629 950 G1198 PRT Arabidopsis thalianaParalogous to G1806, G554, G555, G556, G558, G578, G629 951 G1335 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG652 952 G1335 PRT Arabidopsis thaliana Paralogous to G652 953 G1454 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG1425, G504; orthologous to G3809 954 G1454 PRT Arabidopsis thalianaParalogous to G1425, G504; Orthologous to G3809 955 G1664 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG1062 956 G1664 PRT Arabidopsis thaliana Paralogous to G1062 957 G1897DNA Arabidopsis thaliana Predicted polypeptide sequence is paralogous toG798 958 G1897 PRT Arabidopsis thaliana Paralogous to G798 959 G1991 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG2888 960 G1991 PRT Arabidopsis thaliana Paralogous to G2888 961 G2216DNA Arabidopsis thaliana Predicted polypeptide sequence is paralogous toG2215 962 G2216 PRT Arabidopsis thaliana Paralogous to G2215 963 G2546DNA Arabidopsis thaliana Predicted polypeptide sequence is paralogous toG2550 964 G2546 PRT Arabidopsis thaliana Paralogous to G2550 965 G2586DNA Arabidopsis thaliana Predicted polypeptide sequence is paralogous toG2587, G2686 966 G2586 PRT Arabidopsis thaliana Paralogous to G2587,G2686 967 G2587 DNA Arabidopsis thaliana Predicted polypeptide sequenceis paralogous to G2586, G2686 968 G2587 PRT Arabidopsis thalianaParalogous to G2586, G2686 969 G2635 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G2505 970 G2635 PRT Arabidopsisthaliana Paralogous to G2505 971 G2639 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G2640, G2642 972 G2639PRT Arabidopsis thaliana Paralogous to G2640, G2642 973 G2642 DNAArabidopsis thaliana Predicted polypeptide sequence is paralogous toG2639, G2640 974 G2642 PRT Arabidopsis thaliana Paralogous to G2639,G2640 975 G2721 DNA Arabidopsis thaliana Predicted polypeptide sequenceis paralogous to G1789, G1911, G997 976 G2721 PRT Arabidopsis thalianaParalogous to G1789, G1911, G997 977 G2826 DNA Arabidopsis thalianaPredicted polypeptide sequence is paralogous to G1995, G2838, G361,G362, G370 978 G2826 PRT Arabidopsis thaliana Paralogous to G1995,G2838, G361, G362, G370 979 G2838 DNA Arabidopsis thaliana Predictedpolypeptide sequence is paralogous to G1995, G2826, G361, G362, G370 980G2838 PRT Arabidopsis thaliana Paralogous to G1995, G2826, G361, G362,G370 981 G2866 DNA Arabidopsis thaliana Predicted polypeptide sequenceis paralogous to G468 982 G2866 PRT Arabidopsis thaliana Paralogous toG468 983 G3503 DNA Oryza sativa Predicted polypeptide sequence isparalogous to G3504, G3505, G3506, G3507, G3508; orthologous to G197,G255, G664, G3509, G3529, G3531, G3532, G3533, G3534, G3527, G3528 984G3503 PRT Oryza sativa Paralogous to G3504, G3505, G3506, G3507, G3508;Orthologous to G197, G255, G664, G3509, G3529, G3531, G3532, G3533,G3534, G3527, G3528 985 G3504 DNA Oryza sativa Predicted polypeptidesequence is paralogous to G3503, G3505, G3506, G3507, G3508; orthologousto G197, G255, G664, G3509, G3529, G3531, G3532, G3533, G3534, G3527,G3528 986 G3504 PRT Oryza sativa Paralogous to G3503, G3505, G3506,G3507, G3508; Orthologous to G197, G255, G664, G3509, G3529, G3531,G3532, G3533, G3534, G3527, G3528 987 G3505 DNA Oryza sativa Predictedpolypeptide sequence is paralogous to G3503, G3504, G3506, G3507, G3508;orthologous to G197, G255, G664, G3509, G3529, G3531, G3532, G3533,G3534, G3527, G3528 988 G3505 PRT Oryza sativa Paralogous to G3503,G3504, G3506, G3507, G3508; Orthologous to G197, G255, G664, G3509,G3529, G3531, G3532, G3533, G3534, G3527, G3528 989 G3506 DNA Oryzasativa Predicted polypeptide sequence is paralogous to G3503, G3504,G3505, G3507, G3508; orthologous to G197, G255, G664, G3509, G3529,G3531, G3532, G3533, G3534, G3527, G3528 990 G3506 PRT Oryza sativaParalogous to G3503, G3504, G3505, G3507, G3508; Orthologous to G197,G255, G664, G3509, G3529, G3531, G3532, G3533, G3534, G3527, G3528 991G3507 DNA Oryza sativa Predicted polypeptide sequence is paralogous toG3503, G3504, G3505, G3506, G3508; orthologous to G197, G255, G664,G3509, G3529, G3531, G3532, G3533, G3534, G3527, G3528 992 G3507 PRTOryza sativa Paralogous to G3503, G3504, G3505, G3506, G3508;Orthologous to G197, G255, G664, G3509, G3529, G3531, G3532, G3533,G3534, G3527, G3528 993 G3508 DNA Oryza sativa Predicted polypeptidesequence is paralogous to G3503, G3504, G3505, G3506, G3507; orthologousto G197, G255, G664, G3509, G3529, G3531, G3532, G3533, G3534, G3527,G3528 994 G3508 PRT Oryza sativa Paralogous to G3503, G3504, G3505,G3506, G3507; Orthologous to G197, G255, G664, G3509, G3529, G3531,G3532, G3533, G3534, G3527, G3528 995 G3509 DNA Lycopersicon Predictedpolypeptide sequence is esculentum orthologous to G197, G255, G664,G3503, G3504, G3505, G3506, G3507, G3508, G3529, G3531, G3532, G3533,G3534, G3527, G3528 996 G3509 PRT Lycopersicon Orthologous to G197,G255, G664, esculentum G3503, G3504, G3505, G3506, G3507, G3508, G3529,G3531, G3532, G3533, G3534, G3527, G3528 997 G3527 DNA Glycine maxPredicted polypeptide sequence is paralogous to G3529, G3528;orthologous to G197, G255, G664, G3503, G3504, G3505, G3506, G3507,G3508, G3509, G3531, G3532, G3533, G3534 998 G3527 PRT Glycine maxParalogous to G3529, G3528; Orthologous to G197, G255, G664, G3503,G3504, G3505, G3506, G3507, G3508, G3509, G3531, G3532, G3533, G3534 999G3528 DNA Glycine max Predicted polypeptide sequence is paralogous toG3529, G3527; orthologous to G197, G255, G664, G3503, G3504, G3505,G3506, G3507, G3508, G3509, G3531, G3532, G3533, G3534 1000 G3528 PRTGlycine max Paralogous to G3529, G3527; Orthologous to G197, G255, G664,G3503, G3504, G3505, G3506, G3507, G3508, G3509, G3531, G3532, G3533,G3534 1001 G3529 DNA Glycine max Predicted polypeptide sequence isparalogous to G3527, G3528; orthologous to G197, G255, G664, G3503,G3504, G3505, G3506, G3507, G3508, G3509, G3531, G3532, G3533, G35341002 G3529 PRT Glycine max Paralogous to G3527, G3528; Orthologous toG197, G255, G664, G3503, G3504, G3505, G3506, G3507, G3508, G3509,G3531, G3532, G3533, G3534 1003 G3531 DNA Zea mays Predicted polypeptidesequence is paralogous to G3532, G3533, G3534; orthologous to G197,G255, G664, G3503, G3504, G3505, G3506, G3507, G3508, G3509, G3529,G3527, G3528 1004 G3531 PRT Zea mays Paralogous to G3532, G3533, G3534;Orthologous to G197, G255, G664, G3503, G3504, G3505, G3506, G3507,G3508, G3509, G3529, G3527, G3528 1005 G3532 DNA Zea mays Predictedpolypeptide sequence is paralogous to G3531, G3533, G3534; orthologousto G197, G255, G664, G3503, G3504, G3505, G3506, G3507, G3508, G3509,G3529, G3527, G3528 1006 G3532 PRT Zea mays Paralogous to G3531, G3533,G3534; Orthologous to G197, G255, G664, G3503, G3504, G3505, G3506,G3507, G3508, G3509, G3529, G3527, G3528 1007 G3533 DNA Zea maysPredicted polypeptide sequence is paralogous to G3531, G3532, G3534;orthologous to G197, G255, G664, G3503, G3504, G3505, G3506, G3507,G3508, G3509, G3529, G3527, G3528 1008 G3533 PRT Zea mays Paralogous toG3531, G3532, G3534; Orthologous to G197, G255, G664, G3503, G3504,G3505, G3506, G3507, G3508, G3509, G3529, G3527, G3528 1009 G3534 DNAZea mays Predicted polypeptide sequence is paralogous to G3531, G3532,G3533; orthologous to G197, G255, G664, G3503, G3504, G3505, G3506,G3507, G3508, G3509, G3529, G3527, G3528 1010 G3534 PRT Zea maysParalogous to G3531, G3532, G3533; Orthologous to G197, G255, G664,G3503, G3504, G3505, G3506, G3507, G3508, G3509, G3529, G3527, G35281011 G3809 DNA Oryza sativa Predicted polypeptide sequence isorthologous to G1425, G1454, G504 1012 G3809 PRT Oryza sativaOrthologous to G1425, G1454, G504

Molecular Modeling

Another means that may be used to confirm the utility and function oftranscription factor sequences that are orthologous or paralogous topresently disclosed transcription factors is through the use ofmolecular modeling software. Molecular modeling is routinely used topredict polypeptide structure, and a variety of protein structuremodeling programs, such as “Insight II” (Accelrys, Inc.) arecommercially available for this purpose. Modeling can thus be used topredict which residues of a polypeptide can be changed without alteringfunction (Crameri et al. (2003) U.S. Pat. No. 6,521,453). Thus,polypeptides that are sequentially similar can be shown to have a highlikelihood of similar function by their structural similarity, whichmay, for example, be established by comparison of regions ofsuperstructure. The relative tendencies of amino acids to form regionsof superstructure (for example, helixes and (3-sheets) are wellestablished. For example, O'Neil et al. ((1990) Science 250: 646-651)have discussed in detail the helix forming tendencies of amino acids.Tables of relative structure forming activity for amino acids can beused as substitution tables to predict which residues can befunctionally substituted in a given region, for example, in DNA-bindingdomains of known transcription factors and equivalogs. Homologs that arelikely to be functionally similar can then be identified.

Of particular interest is the structure of a transcription factor in theregion of its conserved domains, such as those identified in Table 1 andTable 3. Structural analyses may be performed by comparing the structureof the known transcription factor around its conserved domain with thoseof orthologs and paralogs. Analysis of a number of polypeptides within atranscription factor group or clade, including the functionally orsequentially similar polypeptides provided in the Sequence Listing, mayalso provide an understanding of structural elements required toregulate transcription within a given family.

EXAMPLES

The invention, now being generally described, will be more readilyunderstood by reference to the following examples, which are includedmerely for purposes of illustration of certain aspects and embodimentsof the present invention and are not intended to limit the invention. Itwill be recognized by one of skill in the art that a transcriptionfactor that is associated with a particular first trait may also beassociated with at least one other, unrelated and inherent second traitwhich was not predicted by the first trait.

The complete descriptions of the traits associated with eachpolynucleotide of the invention are fully disclosed in Examples VIII, IXand X.

Example I: Full Length Gene Identification and Cloning

Putative transcription factor sequences (genomic or ESTs) related toknown transcription factors were identified in the Arabidopsis thalianaGenBank database using the tblastn sequence analysis program usingdefault parameters and a P-value cutoff threshold of −4 or −5 or lower,depending on the length of the query sequence. Putative transcriptionfactor sequence hits were then screened to identify those containingparticular sequence strings. If the sequence hits contained suchsequence strings, the sequences were confirmed as transcription factors.

Alternatively, Arabidopsis thaliana cDNA libraries derived fromdifferent tissues or treatments, or genomic libraries were screened toidentify novel members of a transcription family using a low stringencyhybridization approach. Probes were synthesized using gene specificprimers in a standard PCR reaction (annealing temperature 60° C.) andlabeled with ³²P dCTP using the High Prime DNA Labeling Kit (RocheDiagnostics Corp., Indianapolis, Ind.). Purified radiolabelled probeswere added to filters immersed in Church hybridization medium (0.5 MNaPO₄ pH 7.0, 7% SDS, 1% w/v bovine serum albumin) and hybridizedovernight at 60° C. with shaking. Filters were washed two times for 45to 60 minutes with 1×SCC, 1% SDS at 60° C.

To identify additional sequence 5′ or 3′ of a partial cDNA sequence in acDNA library, 5′ and 3′ rapid amplification of cDNA ends (RACE) wasperformed using the MARATHON cDNA amplification kit (Clontech, PaloAlto, Calif.). Generally, the method entailed first isolating poly(A)mRNA, performing first and second strand cDNA synthesis to generatedouble-stranded cDNA, blunting cDNA ends, followed by ligation of theMARATHON Adaptor to the cDNA to form a library of adaptor-ligated dscDNA.

Gene-specific primers were designed to be used along with adaptorspecific primers for both 5′ and 3′ RACE reactions. Nested primers,rather than single primers, were used to increase PCR specificity. Using5′ and 3′ RACE reactions, 5′ and 3′ RACE fragments were obtained,sequenced and cloned. The process can be repeated until 5′ and 3′ endsof the full-length gene were identified. Then the full-length cDNA wasgenerated by PCR using primers specific to 5′ and 3′ ends of the gene byend-to-end PCR.

Example II: Construction of Expression Vectors

The sequence was amplified from a genomic or cDNA library using primersspecific to sequences upstream and downstream of the coding region. Theexpression vector was pMEN20 or pMEN65, which are both derived frompMON316 (Sanders et al. (1987) Nucleic Acids Res. 15:1543-1558) andcontain the CaMV 35S promoter to express transgenes. To clone thesequence into the vector, both pMEN20 and the amplified DNA fragmentwere digested separately with SalI and NotI restriction enzymes at 37°C. for 2 hours. The digestion products were subject to electrophoresisin a 0.8% agarose gel and visualized by ethidium bromide staining. TheDNA fragments containing the sequence and the linearized plasmid wereexcised and purified by using a QIAQUICK gel extraction kit (Qiagen,Valencia Calif.). The fragments of interest were ligated at a ratio of3:1 (vector to insert). Ligation reactions using T4 DNA ligase (NewEngland Biolabs, Beverly Mass.) were carried out at 16° C. for 16 hours.The ligated DNAs were transformed into competent cells of the E. colistrain DH5a by using the heat shock method. The transformations wereplated on LB plates containing 50 mg/l kanamycin (Sigma Chemical Co. St.Louis Mo.). Individual colonies were grown overnight in five millilitersof LB broth containing 50 mg/l kanamycin at 37° C. Plasmid DNA waspurified by using Qiaquick Mini Prep kits (Qiagen).

Example III: Transformation of Agrobacterium with the Expression Vector

After the plasmid vector containing the gene was constructed, the vectorwas used to transform Agrobacterium tumefaciens cells expressing thegene products. The stock of Agrobacterium tumefaciens cells fortransformation was made as described by Nagel et al. (1990) FEMSMicrobiol Letts. 67: 325-328. Agrobacterium strain ABI was grown in 250ml LB medium (Sigma) overnight at 28° C. with shaking until anabsorbance over 1 cm at 600 nm (A₆₀₀) of 0.5-1.0 was reached. Cells wereharvested by centrifugation at 4,000×g for 15 min at 4° C. Cells werethen resuspended in 250 μl chilled buffer (1 mM HEPES, pH adjusted to7.0 with KOH). Cells were centrifuged again as described above andresuspended in 125 μl chilled buffer. Cells were then centrifuged andresuspended two more times in the same HEPES buffer as described aboveat a volume of 100 μl and 750 respectively. Resuspended cells were thendistributed into 40 μl aliquots, quickly frozen in liquid nitrogen, andstored at −80° C.

Agrobacterium cells were transformed with plasmids prepared as describedabove following the protocol described by Nagel et al. (1990) supra. Foreach DNA construct to be transformed, 50-100 ng DNA (generallyresuspended in 10 mM Tris-HCl, 1 mM EDTA, pH 8.0) was mixed with 40 μlof Agrobacterium cells. The DNA/cell mixture was then transferred to achilled cuvette with a 2 mm electrode gap and subject to a 2.5 kV chargedissipated at 25 μF and 200 μF using a Gene Pulser II apparatus(Bio-Rad, Hercules, Calif.). After electroporation, cells wereimmediately resuspended in 1.0 ml LB and allowed to recover withoutantibiotic selection for 2-4 hours at 28° C. in a shaking incubator.After recovery, cells were plated onto selective medium of LB brothcontaining 100 μg/ml spectinomycin (Sigma) and incubated for 24-48 hoursat 28° C. Single colonies were then picked and inoculated in freshmedium. The presence of the plasmid construct was verified by PCRamplification and sequence analysis.

Example IV: Transformation of Arabidopsis Plants with Agrobacteriumtumefaciens with Expression Vector

After transformation of Agrobacterium tumefaciens with plasmid vectorscontaining the gene, single Agrobacterium colonies were identified,propagated, and used to transform Arabidopsis plants. Briefly, 500 mlcultures of LB medium containing 50 mg/l kanamycin were inoculated withthe colonies and grown at 28° C. with shaking for 2 days until anoptical absorbance at 600 nm wavelength over 1 cm (A₆₀₀) of >2.0 isreached. Cells were then harvested by centrifugation at 4,000×g for 10min, and resuspended in infiltration medium (½×Murashige and Skoog salts(Sigma), 1× Gamborg's B-5 vitamins (Sigma), 5.0% (w/v) sucrose (Sigma),0.044 μM benzylamino purine (Sigma), 200 μl/l Silwet L-77 (Lehle Seeds))until an A₆₀₀ of 0.8 was reached.

Prior to transformation, Arabidopsis thaliana seeds (ecotype Columbia)were sown at a density of −10 plants per 4″ pot onto Pro-Mix BX pottingmedium (Hummert International) covered with fiberglass mesh (18 mm×16mm). Plants were grown under continuous illumination (50-75 μE/m²/sec)at 22-23° C. with 65-70% relative humidity. After about 4 weeks, primaryinflorescence stems (bolts) are cut off to encourage growth of multiplesecondary bolts. After flowering of the mature secondary bolts, plantswere prepared for transformation by removal of all siliques and openedflowers.

The pots were then immersed upside down in the mixture of Agrobacteriuminfiltration medium as described above for 30 sec, and placed on theirsides to allow draining into a 1′×2′ flat surface covered with plasticwrap. After 24 h, the plastic wrap was removed and pots are turnedupright. The immersion procedure was repeated one week later, for atotal of two immersions per pot. Seeds were then collected from eachtransformation pot and analyzed following the protocol described below.

Example V: Identification of Arabidopsis Primary Transformants

Seeds collected from the transformation pots were sterilized essentiallyas follows. Seeds were dispersed into in a solution containing 0.1%(v/v) Triton X-100 (Sigma) and sterile water and washed by shaking thesuspension for 20 min. The wash solution was then drained and replacedwith fresh wash solution to wash the seeds for 20 min with shaking.After removal of the ethanol/detergent solution, a solution containing0.1% (v/v) Triton X-100 and 30% (v/v) bleach (CLOROX; Clorox Corp.Oakland Calif.) was added to the seeds, and the suspension was shakenfor 10 min. After removal of the bleach/detergent solution, seeds werethen washed five times in sterile distilled water. The seeds were storedin the last wash water at 4° C. for 2 days in the dark before beingplated onto antibiotic selection medium (1× Murashige and Skoog salts(pH adjusted to 5.7 with 1M KOH), 1× Gamborg's B-5 vitamins, 0.9%phytagar (Life Technologies), and 50 mg/l kanamycin). Seeds weregerminated under continuous illumination (50-75 μE/m²/sec) at 22-23° C.After 7-10 days of growth under these conditions, kanamycin resistantprimary transformants (T1 generation) were visible and obtained. Theseseedlings were transferred first to fresh selection plates where theseedlings continued to grow for 3-5 more days, and then to soil (Pro-MixBX potting medium).

Primary transformants were crossed and progeny seeds (T2) collected;kanamycin resistant seedlings were selected and analyzed. The expressionlevels of the recombinant polynucleotides in the transformants variesfrom about a 5% expression level increase to a least a 100% expressionlevel increase. Similar observations are made with respect topolypeptide level expression.

Example VI: Identification of Arabidopsis Plants with TranscriptionFactor Gene Knockouts

The screening of insertion mutagenized Arabidopsis collections for nullmutants in a known target gene was essentially as described in Krysan etal. (1999) Plant Cell 11: 2283-2290. Briefly, gene-specific primers,nested by 5-250 base pairs to each other, were designed from the 5′ and3′ regions of a known target gene. Similarly, nested sets of primerswere also created specific to each of the T-DNA or transposon ends (the“right” and “left” borders). All possible combinations of gene specificand T-DNA/transposon primers were used to detect by PCR an insertionevent within or close to the target gene. The amplified DNA fragmentswere then sequenced which allows the precise determination of theT-DNA/transposon insertion point relative to the target gene. Insertionevents within the coding or intervening sequence of the genes weredeconvoluted from a pool comprising a plurality of insertion events to asingle unique mutant plant for functional characterization. The methodis described in more detail in Yu and Adam, U.S. application Ser. No.09/177,733 filed Oct. 23, 1998.

Example VII: Identification of Modified Phenotypes in Overexpression orGene Knockout Plants

Arabidopsis thaliana ecotype Columbia (Col-0) was used to create alloverexpressing lines. The control plants for the assay were Col-0 plantstransformed with an empty transformation vector (pMEN65).

Microarray Experiments

In some instances, expression patterns of the stress-induced genes maybe monitored by microarray experiments. In these experiments, cDNAs aregenerated by PCR and resuspended at a final concentration of 100 ng/μlin 3×SSC or 150 mM Na-phosphate (Eisen and Brown (1999) Methods Enzymol.303: 179-205). The cDNAs are spotted on microscope glass slides coatedwith polylysine. The prepared cDNAs are aliquoted into 384 well platesand spotted on the slides using, for example, an x-y-z gantry (OmniGrid)which may be purchased from GeneMachines (Menlo Park, Calif.) outfittedwith quill type pins which may be purchased from Telechem International(Sunnyvale, Calif.). After spotting, the arrays are cured for a minimumof one week at room temperature, rehydrated and blocked following theprotocol recommended by Eisen and Brown (1999) supra.

Sample total RNA (10 μg) samples are labeled using fluorescent Cy3 andCy5 dyes. Labeled samples are resuspended in 4×SSC/0.03% SDS/4 μg salmonsperm DNA/2 μg tRNA/50 mM Na-pyrophosphate, heated for 95° C. for 2.5minutes, spun down and placed on the array. The array is then coveredwith a glass coverslip and placed in a sealed chamber. The chamber isthen kept in a water bath at 62° C. overnight. The arrays are washed asdescribed in Eisen and Brown (1999) supra) and scanned on a GeneralScanning 3000 laser scanner. The resulting files are subsequentlyquantified using IMAGENE, software (BioDiscovery, Los Angeles Calif.).

RT-PCR experiments may be performed to identify those genes inducedafter exposure to abiotic stresses. Generally, the gene expressionpatterns from ground plant leaf tissue is examined.

Reverse transcriptase PCR was conducted using gene specific primerswithin the coding region for each sequence identified. The primers weredesigned near the 3′ region of each DNA binding sequence initiallyidentified.

Total RNA from these ground leaf tissues was isolated using the CTABextraction protocol. Once extracted total RNA was normalized inconcentration across all the tissue types to ensure that the PCRreaction for each tissue received the same amount of cDNA template usingthe 28S band as reference. Poly(A+) RNA was purified using a modifiedprotocol from the Qiagen OLIGOTEX purification kit batch protocol. cDNAwas synthesized using standard protocols. After the first strand cDNAsynthesis, primers for Actin 2 were used to normalize the concentrationof cDNA across the tissue types. Actin 2 is found to be constitutivelyexpressed in fairly equal levels across the tissue types beinginvestigated.

For RT PCR, cDNA template was mixed with corresponding primers and TaqDNA polymerase. Each reaction consisted of 0.2 μl cDNA template, 2 μl10× Tricine buffer, 2 μl 10× Tricine buffer and 16.8 μl water, 0.05 μlPrimer 1, 0.05 Primer 2, 0.3 μl Taq DNA polymerase and 8.6 μl water.

The 96 well plate is covered with microfilm and set in the thermocyclerto start the reaction cycle. By way of illustration, the reaction cyclemay comprise the following steps:

STEP 1: 93° C. for 3 minutes;

STEP 2: 93° C. for 30 seconds;

STEP 3: 65° C. for 1 minute;

STEP 4: 72° C. for 2 minutes;

STEPS 2, 3 and 4 are repeated for 28 cycles;

STEP 5: 72° C. for 5 minutes; and

STEP 6 4° C.

To amplify more products, for example, to identify genes that have verylow expression, additional steps may be performed: the following methodillustrates a method that may be used in this regard. the PCR plate isplaced back in the thermocycler for 8 more cycles of Steps 2-4.

STEP 2 93° C. for 30 seconds;

STEP 3 65° C. for 1 minute;

STEP 4 72° C. for 2 minutes, repeated for 8 cycles; and

STEP 5 4° C.

Eight microliters of PCR product and 1.5 μl of loading dye are loaded ona 1.2% agarose gel for analysis after 28 cycles and 36 cycles.Expression levels of specific transcripts are considered low if theywere only detectable after 36 cycles of PCR. Expression levels areconsidered medium or high depending on the levels of transcript comparedwith observed transcript levels for an internal control such as actin2.Transcript levels are determined in repeat experiments and compared totranscript levels in control (e.g., non-transformed) plants.

Abiotic Stress Assays

Modified phenotypes observed for particular overexpressor plants mayinclude increased biomass, and/or increased or decreased abiotic stresstolerance or resistance. For a particular overexpressor that shows aless beneficial characteristic, such as reduced abiotic stress toleranceor resistance, it may be more useful to select a plant with a decreasedexpression of the particular transcription factor. For a particularknockout that shows a less beneficial characteristic, such as decreasedabiotic stress tolerance, it may be more useful to select a plant withan increased expression of the particular transcription factor.

The germination assays in this example followed modifications of thesame basic protocol. Sterile seeds were sown on the conditional medialisted below. Plates were incubated at 22° C. under 24-hour light(120-130 μEin/m²/s) in a growth chamber. Evaluation of germination andseedling vigor was conducted 3 to 15 days after planting. The basalmedia was 80% Murashige-Skoog medium (MS)+vitamins.

For stress experiments conducted with more mature plants, seeds weregerminated and grown for seven days on MS+vitamins+1% sucrose at 22° C.and then transferred to cold and heat stress conditions. The plants wereeither exposed to cold stress (6 hour exposure to 4-8° C.), or heatstress (32° C. was applied for five days, after which the plants weretransferred back 22° C. for recovery and evaluated after 5 days relativeto controls not exposed to the depressed or elevated temperature).

The salt stress assays were intended to find genes that confer bettergermination, seedling vigor or growth in high salt. Evaporation from thesoil surface causes upward water movement and salt accumulation in theupper soil layer where the seeds are placed. Thus, germination normallytakes place at a salt concentration much higher than the mean saltconcentration of in the whole soil profile. Plants differ in theirtolerance to NaCl depending on their stage of development, thereforeseed germination, seedling vigor, and plant growth responses wereevaluated.

Osmotic stress assays (including NaCl and mannitol assays) wereconducted to determine if an osmotic stress phenotype was NaCl-specificor if it was a general osmotic stress related phenotype. Plants tolerantto osmotic stress could also have more tolerance to drought and/orfreezing.

For salt and osmotic stress germination experiments, the medium wassupplemented with 150 mM NaCl or 300 mM mannitol. Growth regulatorsensitivity assays were performed in MS media, vitamins, and either 0.3μM ABA, 9.4% sucrose, or 5% glucose.

Experiments were performed to identify those transformants thatexhibited modified sugar-sensing. For such studies, seeds fromtransformants were germinated on high sugar-containing media (5%glucose, 9.4% sucrose) that normally partially restrict hypocotylelongation. Plants with altered sugar sensing may have either longer orshorter hypocotyls than normal plants when grown on this media.Additionally, other plant traits may be varied such as root mass. Sugarsensing assays were intended to find genes involved in sugar sensing bygerminating seeds on high concentrations of sucrose and glucose andlooking for degrees of hypocotyl elongation. The germination assay onmannitol controlled for responses related to osmotic stress. Sugars arekey regulatory molecules that affect diverse processes in higher plantsincluding germination, growth, flowering, senescence, sugar metabolismand photosynthesis. Sucrose is the major transport form of photosynthateand its flux through cells has been shown to affect gene expression andalter storage compound accumulation in seeds (source-sinkrelationships). Glucose-specific hexose-sensing has also been describedin plants and is implicated in cell division and repression of “famine”genes (photosynthetic or glyoxylate cycles).

Temperature stress assays were carried out to find genes that conferbetter germination, seedling vigor or plant growth under temperaturestress (cold, freezing and heat). Temperature stress cold germinationexperiments were carried out at 8° C. Heat stress germinationexperiments were conducted at 32° C. to 37° C. for 6 hours of exposure.

Soil-based drought screens were performed with Arabidopsis plantsoverexpressing the transcription factors listed in the Sequence Listing.Seeds from wild-type Arabidopsis plants, or plants overexpressing apolypeptide of the invention, were stratified for three days at 4° C. in0.1% agarose. Fourteen seeds of each overexpressor or wild-type werethen sown in three inch clay pots containing a 50:50 mix ofvermiculite:perlite topped with a small layer of MetroMix 200 and grownfor fifteen days under 24 hr light. Pots containing wild-type andoverexpressing seedlings were placed in flats in random order. Droughtstress was initiated by placing pots on absorbent paper for seven toeight days. The seedlings were considered to be sufficiently stressedwhen the majority of the pots containing wild-type seedlings within aflat had become severely wilted. Pots were then re-watered and survivalwas scored four to seven days later. Plants were ranked againstwild-type controls for each of two criteria: tolerance to the droughtconditions and recovery (survival) following re-watering

At the end of the initial drought period, each pot was assigned anumeric value score depending on the above criteria. Scores of 0-6 wereassigned (Table 11), with a low value of “0” assigned to plants with anextremely poor appearance (i.e., the plants were uniformly brown) and avalue of “6” given to plants that were rated very healthy in appearance(i.e., the plants were all green). After the plants were rewatered andincubated an additional four to seven days, the plants were reevaluatedto indicate the degree of recovery from the water deprivation treatment.

An analysis was then conducted to determine which plants best survivedwater deprivation, identifying the transgenes that consistentlyconferred drought-tolerant phenotypes and their ability to recover fromthis treatment. The analysis was performed by comparing overall andwithin-flat tabulations with a set of statistical models to account forvariations between batches. Several measures of survival were tabulated,including: (a) the average proportion of plants surviving relative towild-type survival within the same flat; (b) the median proportionsurviving relative to wild-type survival within the same flat; (c) theoverall average survival (taken over all batches, flats, and pots); (d)the overall average survival relative to the overall wild-type survival;and (e) the average visual score of plant health before rewatering.

Analysis of Flowering Time

Flowering time was measured by the number of rosette leaves present whena visible inflorescence of approximately 3 cm is apparent. Rosette andtotal leaf number on the progeny stem are tightly correlated with thetiming of flowering (Koornneef et al. (1991) Mol. Gen. Genet. 229:57-66). The vernalization response was also measured. For vernalizationtreatments, seeds were sown to MS agar plates, sealed with microporetape, and placed in a 4° C. cold room with low light levels for 6-8weeks. The plates were then transferred to the growth rooms alongsideplates containing freshly sown non-vernalized controls. Rosette leaveswere counted when a visible inflorescence of approximately 3 cm wasapparent.

C/N Sensing Assays

Germination assays were conducted to monitor the effects of C on Nsignaling through anthocyanin production on high sucrose plus and minusglutamine (Hsieh et al, (1998) Proc. Natl. Acad. Sci. USA. 95:13965-13970).

For overexpression lines examined in the assay, the screen was primarilyperformed on a seed lot comprised of seed mixed together from each ofthree independent primary transformants. These seed batches weresegregating, but selection was not performed to avoid the extra stressthat might be associated with kanamycin selection. In the case ofknockout (KO) lines, the screen was performed on seed from plant(s)homozygous for a T-DNA insertion within the gene of interest. Lines thatgave positive results in our previous studies were included here aspositive controls.

All assays were designed to detect plants that were more tolerant orless tolerant of an alteration in C/N balance brought about by anincrease in sucrose levels in the absence of a nitrogen source. Lineswere scored as tolerant if they accumulated lower levels of anthocyaninsthan controls and sensitive if they accumulated higher levels ofanthocyanins than controls. The general vigor and size of the seedlingscompared to controls was also assessed.

Prior to plating, seed for all experiments were surface sterilized andprepared for germination by:

1. a 5 minute incubation with mixing in 70% ethanol;

2. a 20 minute incubation with mixing in 30% bleach, 0.01% triton-X 100;

3. five rinses with sterile water; and

4. seeds are re-suspended in 0.1% sterile agarose and stratified at 4°C. for 3 days.

The sterile seeds were then sown onto plates containing media based on80% MS without a nitrogen source. For C/N assays, the media contained 3%sucrose. The −N/+Gln media was identical but was supplemented with 1 mMglutamine. Plates were incubated in a 24-hour light C (120-130 μEins⁻²m⁻¹) growth chamber at 22° C. Evaluation of germination and seedlingvigor was done five days after planting for C/N assays. The productionof less anthocyanin on these media is generally associated withincreased tolerance to nitrogen limitation, and a transgene responsiblefor the altered response is likely involved in the plant's ability toperceive their carbon and nitrogen status.

Data was recorded for all phenotypes observed, regardless of theirstrength, based on the assumption that any lead could potentially resultin a product either after a period of development or improvement, orwhen used in combination with another gene involved in the particularstress response pathway.

All scores presented in the result lists (other than wild-type) werebased on data from two independent experiments on the seed batches,assuming sufficient seed was available to repeat the experiment twice.

Shade Tolerance Assays

The shade avoidance response was determined by the perception of lightquality. We used an assay which detects alterations in the mechanismsthat plants use to sense light quality and presumably activate thesignal transduction cascades that regulate a shade avoidance response.Seeds were germinated under white light versus light deficient in thered portion of the visible spectrum. In a natural setting, reflected ortransmitted light would be deficient in both the red and blue portionsof the visible spectrum. However, because shading is detected usingphytochrome to sense the R:FR ratio in light, we mimicked the effect ofshading by using a filter designed to prevent only the transmission ofred wavelengths (to mimic loss of red light caused by shading). Todetermine whether the mechanisms used to sense shading were altered, weexploited the observation that seedlings of wild-type plants grown underlight deficient in red wavelengths have extended hypocotyls. Plantsoverexpressing genes that produce short hypocotyls under theseconditions and exhibit a shade tolerance phenotype are candidates forfurther examination in more rigorous studies looking at components suchas yield under high densities in greenhouse studies.

The assay was intended to associate a transcription factor with shadeavoidance control mechanisms. All data were recorded, regardless ofphenotype strength, based on the assumption that any lead (or itsrelated paralogs/orthologs) could potentially result in a product eitherafter a period of development or improvement, or when used incombination with another gene involved in the particular stress responsepathway.

Arabidopsis thaliana ecotype Columbia (Col-0) was used to create alloverexpressing lines. The control plants for the assay were Col-0 plantstransformed with an empty transformation vector (pMEN65).

For overexpression lines examined in the assay, the screen was primarilyperformed on a seed lot comprised of seed mixed together from each ofthree independent primary transformants. These seed batches weresegregating, but selection was not performed to avoid the extra stressthat might be associated with kanamycin selection. In the case ofknockout (KO) lines, the screen was performed on seed from plant(s)homozygous for a T-DNA insertion within the gene of interest.

Prior to plating, seed for all experiments were surface sterilized inthe following manner:

1. 5 minute incubation with mixing in 70% ethanol

2. 20 minute incubation with mixing in 30% bleach, 0.01% triton-X 100

3. 5× rinses with sterile water

4. Seeds are re-suspended in 0.1% sterile agarose and stratified at 4°C. for 3 days.

The basal media onto which Arabidopsis seeds were plated comprised 80%MS+Vitamins. For shade avoidance assays, plates were incubated at 22° C.under 24-hour light (about 50 μEinsteins⁻² m⁻¹) under both white light(control) and under light depleted in red wavelengths. Seedlings weregrown in a chamber deficient in red light versus a standard white lightchamber. The assay was designed to detect plants that were more tolerantof the low R:FR conditions. The growth chamber used in the shadeavoidance screen contained a filter that effectively removed wavelengthsin the red region of the visible light spectrum. Seedlings were assessedfor shade tolerance at 7 days.

Shade tolerance was scored by visually observing differences inhypocotyl length compared with control seedlings grown under white lightand grown under light lacking the red wavelengths.

Examples of genes and homologs that confer significant improvements toknockout or overexpressing plants are noted below. Experimentalobservations made by us with regard to specific genes whose expressionhas been modified in overexpressing or knock-out plants, and potentialapplications based on these observations, are also presented. In mostcases, the conserved domains can be determined and located in each ofthe sequences provided below with the protein BLAST (BLASTp) page of theNCBI Conserved Domain Database, presently found at:blast.ncbi.nlm.nih.gov/Blast.cgi. (Marchler-Bauer A et al. (2009)Nucleic Acids Res. 37(D): 205-210; Marchler-Bauer and Bryant (2004)Nucleic Acids Res. 32(W): 327-331).

Example VIII: Results of Drought Stress Analyses

This example provides experimental evidence for increased abiotic stresstolerance controlled by transcription factor polypeptides andpolypeptides of the invention.

Results:

As noted below, overexpression of G2133, G1274, G922, G2999, G3086,G354, G1792, G2053, G975, G1069, G916, G1820, G2701, G47, G2854, G2789,G634, G175, G2839, G1452, G3083, G489, G303, G2992, and G682 was shownto increase drought stress tolerance in plants. A number of orthologs ofsome of these sequences were also able to increase abiotic stresstolerance, as noted below.

The G47 Clade of Transcription Factor Polypeptides G47 (SEQ ID NO: 1 and2)

G47 corresponds to gene T22J18.2 (AAC25505). No information is availableabout the function(s) of G47. G47 and closely-related clade membersequences each comprise a conserved AP2 DNA binding domain that isexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

The function of G47 was studied using transgenic Arabidopsis plants inwhich the gene was expressed under the control of the 35S promoter.Overexpression of G47 resulted in a variety of morphological andphysiological phenotypic alterations.

35S::G47 plants showed enhanced tolerance to osmotic stress; osmoticstress assays were conducted using growth medium containing polyethyleneglycol (PEG). After germination, the seedlings of 35S::G47overexpressing lines generally appeared larger and had more root growththan wild-type control seedlings.

As would be predicted by these osmotic stress assays, G47 plants alsoshowed enhanced survival and drought tolerance in a soil-based droughtassay.

Overexpression of G47 also produced a substantial delay in floweringtime and caused a marked change in shoot architecture. 35S::G47transformants were small at early stages and switched to flowering morethan a week later than wild-type controls (continuous light conditions).Interestingly, the inflorescences from these plants appeared thick andfleshy, had reduced apical dominance, and exhibited reduced internodeelongation leading to a short compact stature. The branching pattern ofthe stems also appeared abnormal, with the primary shoot becoming‘kinked’ at each coflorescence node. Additionally, the plants showedslightly reduced fertility and formed rather small siliques that wereborne on short pedicels and held vertically, close against the stem.

Additional alterations were detected in the inflorescence stems of35S::G47 plants. Stem sections from T2-21 and T2-24 plants were of widerdiameter, and had large irregular vascular bundles containing a muchgreater number of xylem vessels than wild type. Furthermore some of thexylem vessels within the bundles appeared narrow and were possibly morelignified than were those of controls.

G47 was expressed at higher levels in rosette leaves, and transcriptscan be detected in other tissues (flower, embryo, silique, andgerminating seedling), but apparently not in roots.

Utilities.

G47 or its equivalogs can be used to increase the tolerance of plants todrought and to other osmotic stresses. G47 or its equivalogs could alsobe used to manipulate flowering time, to modify plant architecture andstem structure, including development of vascular tissues and lignincontent. The use of G47 or its equivalogs from tree species could offerthe potential for modulating lignin content. This might allow thequality of wood used for furniture or construction to be improved. G47equivalogs include, for example, Arabidopsis thaliana SEQ ID NO: 12(G2133); Oryza sativa (japonica cultivar-group) SEQ ID NOs: 98 (G3649),SEQ ID NO: 100 (G3651), and SEQ ID NO: 90 (G3644); Glycine max SEQ IDNO: 88 (G3643); Zinnia elegans SEQ ID NO: 96 (G3647); Brassica rapasubsp. Pekinensis SEQ ID NO: 92 (G3645); and Brassica oleracea SEQ IDNO: 94 (G3646).

G2133 (SEQ ID NO: 11 and 12)

G2133 is a paralog of G47. G2133 corresponds to gene F26A9.11(AAF23336). No information is available about the function(s) of G2133.G2133 and closely-related clade member sequences each comprise aconserved AP2 DNA-binding domain that is expected to function in asimilar manner in each of these related sequences, that is, by playing acentral role in transcriptional regulation and in the conferring ofshared traits.

Experimental Observations.

The function of G2133 was studied using transgenic Arabidopsis plants inwhich the gene was expressed under the control of the 35S promoter.

G2133 expression was detected in a variety of tissues: flower, leaf,embryo, and silique samples. Its expression might be altered by severalconditions, including auxin treatment, osmotic stress, and Fusariuminfection. Overexpression of G2133 caused a variety of alterations inplant growth and development: delayed flowering, altered inflorescencearchitecture, and a decrease in overall size and fertility.

At early stages, 35S::G2133 transformants were markedly smaller thancontrols and displayed curled, dark-green leaves. Most of these plantsremained in a vegetative phase of development substantially longer thancontrols, and produced an increased number of leaves before bolting. Inthe most severely affected plants, bolting occurred more than a monthlater than in wild type (24-hour light). In addition, the plantsdisplayed a reduction in apical dominance and formed large numbers ofshoots simultaneously, from the axils of rosette leaves. Theseinflorescence stems had short internodes, and carried increased numbersof cauline leaf nodes, giving them a very leafy appearance. Thefertility of 35S::G2133 plants was generally very low. In addition,G2133 overexpressing lines were found to be more resistant to theherbicide glyphosate in initial and repeat experiments.

No alterations were detected in 35S::G2133 plants in the biochemicalanalyses that were performed.

G2133 is a paralog of G47, the latter having been known from earlierstudies to confer a drought tolerance phenotype when overexpressed. Itwas thus not surprising when G2133 was also shown to induce droughttolerance in a number of 35S::G2133 lines challenged in soil-baseddrought assays (Tables 11 and 12). Experiments comparing the recovery ofwild-type controls and two lines of Arabidopsis plants overexpressingG2133 (a paralog of G47) from a drought treatment were conducted underconstant light. The 35S::G2133 and control lines were grown in pots witheach pot containing several plants. All were deprived of water for eightdays, and then re-watered. After re-watering, all of the plants of bothG2133 overexpressor lines became reinvigorated, and all of the controlplants died or were severely affected by the drought treatment (Table12).

Utilities.

G2133 and its equivalogs can be used to increase the tolerance of plantsto drought and to other osmotic stresses. G2133 could also be used forthe generation of glyphosate resistant plants, and to increase plantresistance to oxidative stress. G2133 equivalogs include, for example,Arabidopsis thaliana SEQ ID NO: 2 (G47); Oryza sativa (japonicacultivar-group) SEQ ID NO: 98 (G3649), SEQ ID NO: 100 (G3651), and SEQID NO: 90 (G3644); Glycine max SEQ ID NO: 88 (G3643); Zinnia elegans SEQID NO: 96 (G3647); Brassica rapa subsp. Pekinensis SEQ ID NO: 92(G3645); and Brassica oleracea SEQ ID NO: 94 (G3646).

G3643 (SEQ ID NO: 87 and 88)

G3643 is a soy ortholog of G47 and G2133. G3643 and closely-relatedclade member sequences each comprise a conserved AP2 DNA-binding domainthat is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

The function of G3643 was studied using transgenic Arabidopsis plants inwhich the gene was expressed under the control of the 35S promoter.

G3643-overexpressing Arabidopsis plants were more tolerant to cold thanwild-type control plants grown under similar conditions in plate-basedgermination assays. One of these lines was also more tolerant todesiccation and growth in cold conditions in plate-based assays.

Utilities.

G3643 or its equivalogs can be used to increase the tolerance of plantsto cold conditions and low water conditions, including drought.

G3644 (SEQ ID NO: 89 and 90)

G3644 is a rice ortholog of G47 and G2133. G3644 and closely-relatedclade member sequences each comprise a conserved AP2 DNA-binding domainthat is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

The function of G3644 was studied using transgenic Arabidopsis plants inwhich the gene was expressed under the control of the 35S promoter.

Several G3644-overexpressing Arabidopsis plants were found to be moretolerant to desiccation than wild-type control plants grown undersimilar conditions in plate based-assays. Two lines were shown to bemore salt tolerant than wild type.

Utilities.

G3644 or its equivalogs can be used to increase the tolerance of plantsto high salt and low water conditions, including drought.

G3649 (SEQ ID NO: 97 and 98)

G3649 is a rice ortholog of G47 and G2133. G3649 and closely-relatedclade member sequences each comprise a conserved AP2 DNA-binding domainthat is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

The function of G3649 was studied using transgenic Arabidopsis plants inwhich the gene was expressed under the control of the 35S promoter.

Several G3649-overexpressing Arabidopsis plants were more tolerant tocold than wild-type control plants grown under similar conditions inplate-based germination assays. Two overexpressing lines were more heattolerant than wild-type plants, and one 35S::G3649 line was found to bemore desiccation tolerant than wild type.

Utilities.

G3649 or its equivalogs can be used to increase the tolerance of plantsto cold conditions and low water conditions, including drought.

The G1274 Clade of Transcription Factor Polypeptides G1274 (SEQ ID NO: 5and 6)

G1274 is a member of the WRKY family of transcription factors. The genecorresponds to WRKY51 (At5g64810). G1274 and closely-related clademember sequences each comprise a conserved WRKY DNA-binding domain thatis expected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR analysis was used to determine the endogenous expression patternof G1274. Expression of G1274 was detected in leaf, root and flowertissues. The biotic stress related conditions, Erysiphe and SAtreatment, induced expression of G1274 in leaf tissue. The gene alsoappeared to be slightly induced by osmotic and cold stress treatmentsand perhaps by auxin.

The function of G1274 was studied using transgenic plants in which thegene was expressed under the control of the 35S promoter. G1274overexpressing lines were more tolerant to growth on low nitrogencontaining media. In an assay intended to determine whether thetransgene expression could alter C/N sensing, 35S::G1274 seedlingscontained less anthocyanins than wild-type controls (grown on highsucrose/N- and high sucrose/N/Gln plates. These data together indicatedthat overexpression of G1274 may alter a plant's ability to modulatecarbon and/or nitrogen uptake and utilization.

G1274 overexpression and wild-type germination were also compared in acold germination assay, the overexpressors appearing larger and greenerthan the controls.

35S::G1274-overexpressing plants were significantly greener and largerthan wild-type control plants in a soil-based drought assay (Tables 11and 12). These assays confirmed the results predicted after theperformance of the plate-based osmotic stress assays; 35S::G1274 linesfared much better after a period of water deprivation than controlplants. This distinction was particularly evident in the overexpressorplants after once again being watered; the overexpressor plants almostall fully recovered to a healthy and vigorous state. Conversely, none ofthe wild-type plants recovered after rewatering, as it was apparentlytoo late for rehydration to rescue these plants (Table 12).

In addition, 35S::G1274 transgenic plants were more tolerant to chillingcompared to the wild-type controls, in both germination as well asseedling growth assays.

Overexpression of G1274 produced alterations in leaf morphology andinflorescence architecture. Four out of eighteen 35S::G1274 primarytransformants were slightly small and developed inflorescences that wereshort, and showed reduced internode elongation, leading to a bushier,more compact stature than in wild-type.

In an experiment using T2 populations, it was observed that the rosetteleaves from many of the plants were distinctly broad and appeared tohave a greater rosette biomass than in wild type.

A similar inflorescence phenotype was obtained from overexpression of apotentially related WRKY gene, G1275. However, G1275 also caused extremedwarfing, which was not apparent when G1274 was overexpressed.

Utilities.

The phenotypic effects of G1274 or equivalog overexpression could haveseveral potential applications:

The enhanced performance of 35S::G1274 plants in a soil-based droughtassay indicated that the gene or its equivalogs may be used to enhancedrought tolerance in plants.

The enhanced performance of 35S::G1274 seedlings under chillingconditions indicates that the gene or its equivalogs might be applied toengineer crops that show better growth under cold conditions.

The morphological phenotype shown by 35S::G1274 lines indicate that thegene or its equivalogs might be used to alter inflorescencearchitecture, to produce more compact dwarf forms that might affordyield benefits.

The effects on leaf size that were observed as a result of G1274 orequivalog overexpression might also have commercial applications.Increased leaf size, or an extended period of leaf growth, couldincrease photosynthetic capacity, and biomass, and have a positiveeffect on yield. G1274 equivalogs include, for example, Arabidopsisthaliana SEQ ID NO: 30 (G1275) and SEQ ID NO: 32 (G1758); Oryza sativa(japonica cultivar-group) SEQ ID NO: 134 (G3721), SEQ ID NO: 142(G3725), SEQ ID NO: 144 (G3726), SEQ ID NO: 150 (G3729), and SEQ ID NO:152 (G3730); Glycine max SEQ ID NO: 138 (G3723), SEQ ID NO: 140 (G3724),and SEQ ID NO: 208 (G3803); Solanum tuberosum SEQ ID NO: 156 (G3732);Capsicum annuum SEQ ID NO: 202 (G3795); Lactuca sativa SEQ ID NO: 204(G3797); Hordeum vulgare SEQ ID NO: 158 (G3733); Zea mays SEQ ID NO: 130(G3719), SEQ ID NO: 132 (G3720), SEQ ID NO: 136 (G3722), SEQ ID NO: 146(G3727), SEQ ID NO: 148 (G3728), and SEQ ID NO: 210 (G3804); Sorghumbicolor SEQ ID NO: 206 (G3802); and Lycopersicon esculentum SEQ ID NO:154 (G3731).

The G922 Clade of Transcription Factor Polypeptides G922 (SEQ ID NO: 3and 4)

G922 corresponds to Scarecrow-like 3 (SCL3) first described by Pysh etal. (GenBank accession number AF036301; (1999) Plant J. 18: 111-119).Northern blot analysis results show that G922 is expressed in siliques,roots, and to a lesser extent in shoot tissue from 14 day old seedlings.Pysh et al did not test any other tissues for G922 expression. In situhybridization results showed that G922 was expressed predominantly inthe endodermis in the root tissue. This pattern of expression was verysimilar to that of SCARECROW (SCR), G306. Experimental evidenceindicated that the co-localization of the expression is not due tocross-hybridization of the G922 probe with G306. Pysh et al proposedthat G922 may play a role in epidermal cell specification and that G922may either regulate or be regulated by G306. G922 and closely-relatedclade member sequences each comprise at least one conserved SCR domainthat is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

The sequence for G922 can also be found in the annotated BAC cloneF11F12 from chromosome 1 (GenBank accession number AC012561). Thesequence for F11F12 was submitted to GenBank by the DNA Sequencing andTechnology Center at Stanford University.

Experimental Observations.

The function of this gene was analyzed using transgenic plants in whichG922 was expressed under the control of the 35S promoter.

Morphologically, plants overexpressing G922 had altered leaf morphology,coloration, fertility, and overall plant size. In wild-type plants,expression of G922 was induced by auxin, ABA, heat, and droughttreatments. In non-induced wild-type plants, G922 was expressedconstitutively at low levels.

Transgenic plants overexpressing G922 were more salt tolerant thanwild-type plants as determined by a root growth assay on MS mediasupplemented with 150 mM NaCl; 35S::G922 overexpressors exhibitedgreener seedlings with longer roots than wild-type seedlings.

G922 overexpressors were more cold tolerant than wild-type controls,with overexpressor lines accumulating less anthocyanin than wild-typeplants.

G922 overexpressors were also more desiccation tolerant in plate-basedassays than wild-type control plants, as the seedlings of the formerwere larger and greener in these experiments.

Almost all of the G922 overexpressors were exhibited a degree ofinsensitivity to ABA; on ABA-containing plates, overexpressor seedlingswere larger and greener than wild-type controls. For some lines, thedifference between overexpressors and wild-type plants was dramatic.

Arabidopsis plants overexpressing G922 also were more tolerant toosmotic stress as determined by germination assays in sucrose(9.4%)-containing media than controls; overexpressors had greenercotyledons and longer roots than wild-type seedlings on the same media.

The high salt, ABA, osmotic stress and plate-based desiccation assayssuggested that this gene would confer drought tolerance, a suppositionconfirmed by soil-based assays, in which G922-overexpressing plants weresignificantly healthier after water deprivation treatment than wild-typecontrol plants (Tables 11 and 12).

Utilities.

Based upon results observed in plants overexpressing G922 or itsequivalogs could be used to alter salt tolerance, tolerance to osmoticstress, and leaf morphology in other plant species. Evaporation from thesoil surface causes upward water movement and salt accumulation in theupper soil layer where the seeds are placed. Thus, germination normallytakes place at a salt concentration much higher than the mean saltconcentration in the whole soil profile. Increased salt tolerance duringthe germination stage of a crop plant would impact survivability andyield.

Altered leaf morphology conferred by overexpression of G922 or itsequivalogs could be desirable in ornamental horticulture. G922equivalogs include, for example, Oryza sativa (japonica cultivar-group)SEQ ID NO: 218 (G3814), SEQ ID NO: 216 (G3813), and SEQ ID NO: 222(G3827); Lycopersicon esculentum SEQ ID NO: 220 (G3824); and Glycine maxSEQ ID NO: 212 (G3810) and SEQ ID NO: 214 (G3811).

The G2999 Clade of Transcription Factor Polypeptides G2999 (SEQ ID NO:13 and 14)

G2999 was identified within a sequence released by the ArabidopsisGenome Initiative (Chromosome 2, GenBank accession AC006439). G2999 andclosely-related clade member sequences each comprise a conserved ZF-HDprotein dimerization domain and a homeo_ZF_HD homeobox domain that areexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

The boundaries of G2999 were determined by RACE experiments and afull-length clone was PCR-amplified out of cDNA derived from mixedtissues. The function of G2999 was then assessed by analysis oftransgenic Arabidopsis lines in which the cDNA was constitutivelyexpressed from a 35S CaMV promoter. 35S::G2999 transformants displayedwild-type morphology, but two of three T2 lines showed increasedtolerance to salt stress. Root growth assays with G2999 overexpressingseedlings and controls in a high sodium chloride medium showed that amajority of 35S::G2999 Arabidopsis seedlings appeared larger, greener,and had more root growth than the control seedlings. G2998, a paralogousArabidopsis sequence, also showed a salt tolerance phenotype in aplate-based salt stress assay, where these overexpressors were greenerand had more cotyledon expansion than wild-type seedlings. Thus, G2998and G2999 could act in the same pathways, and have a role in theresponse to abiotic stress.

G2999 overexpressing lines were also more osmotic stress tolerant, asevidenced by comparing their growth with wild-type plants on 9.4%sucrose, and more cold tolerant than wild-type plants.

These assays suggested that this gene would confer drought tolerance, asupposition confirmed in a soil-based assay in which G2999overexpressing-plants were significantly more drought tolerant thanwild-type control plants (Tables 11 and 12).

Utilities.

Given the pattern of abiotic stress tolerance exhibited by 35S::G2999transformants, the gene and its equivalogs can be used to engineerdrought and salt tolerant crops and trees that can flourish inconditions of osmotic stress. G2999 equivalogs include, for example,Arabidopsis thaliana SEQ ID NO: 50 (G2992), SEQ ID NO: 48 (G2991), SEQID NO: 68 (G3002), SEQ ID NO: 66 (G3001), SEQ ID NO: 46 (G2990), SEQ IDNO: 44 (G2989), SEQ ID NO: 62 (G2998), SEQ ID NO: 64 (G3000), SEQ ID NO:54 (G2994), SEQ ID NO: 52 (G2993), SEQ ID NO: 60 (G2997), SEQ ID NO: 58(G2996), SEQ ID NO: 56 (G2995); Zea mays SEQ ID NO: 114 (G3680); Oryzasativa (japonica cultivar group) SEQ ID NO: 128 (G3695), SEQ ID NO: 126(G3694), SEQ ID NO: 122 (G3690), SEQ ID NO: 118 (G3685), SEQ ID NO: 108(G3671), SEQ ID NO: 116 (G3683), and SEQ ID NO: 124 (G3692); Oryzasativa (indica cultivar group) SEQ ID NO: 120 (G3686) and SEQ ID NO: 110(G3674); Lotus corniculatus var. japonicus SEQ ID NO: 102 (G3663) andSEQ ID NO: 106 (G3670); Brassica napus SEQ ID NO: 112 (G3675); andFlaveria bidentis SEQ ID NO: 104 (G3668).

G2989 (SEQ ID NO: 43 and 44)

G2989 is a paralog of G2999 from Arabidopsis. G2989 and closely-relatedclade member sequences each comprise a conserved ZF-HD proteindimerization domain and a homeo_ZF_HD homeobox domain that are expectedto function in a similar manner in each of these related sequences, thatis, by playing a central role in transcriptional regulation and in theconferring of shared traits.

Experimental Observations.

G2989 overexpressors were more desiccation and cold tolerant thanwild-type controls in plate-based assays.

Utilities.

Given the pattern of abiotic stress tolerance exhibited by 35S::G2989transformants, the gene and its equivalogs can be used to engineerdrought and cold tolerant crops and trees.

G2990 (SEQ ID NO: 45 and 46)

G2990 is a paralog of G2999 from Arabidopsis. G2990 and closely-relatedclade member sequences each comprise a conserved ZF-HD proteindimerization domain and a homeo_ZF_HD homeobox domain that are expectedto function in a similar manner in each of these related sequences, thatis, by playing a central role in transcriptional regulation and in theconferring of shared traits.

Experimental Observations.

G2990 overexpressors were more ABA insensitive and desiccation and coldtolerant than wild-type controls in plate-based assays.

Utilities.

Given the pattern of abiotic stress tolerance exhibited by 35S::G2990transformants, the gene and its equivalogs can be used to engineerdrought and cold tolerant crops and trees.

G2992 (SEQ ID NO: 49 and 50)

G2992 corresponds to gene F24J1.29 within BAC clone F24J1 (GenBankaccession AC021046) derived from chromosome 1. We identified this locusas a novel member of the ZF-HB family and no data regarding its functionare currently in the public domain (as of 8/5/02). G2992 andclosely-related clade member sequences each comprise a conserved ZF-HDprotein dimerization domain and a homeo_ZF_HD homeobox domain that areexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

The boundaries of G2992 were determined by RACE, and a clone wasPCR-amplified from cDNA derived from mixed tissue samples. The functionof G2992 was then assessed by analysis of transgenic Arabidopsis linesin which the cDNA was constitutively expressed from a 35S CaMV promoter.

Morphological studies revealed that overexpression of G2992 canaccelerate the onset of reproductive development, reduce plant size, andproduce changes in leaf shape.

35S::G2992 T2 populations displayed an enhanced ability to germinate onplates containing high levels of sodium chloride. The role of G2992 in aresponse pathway to abiotic stress was affirmed by a soil-based droughtassay, in which it was shown that G2992 overexpressors were, on average,more tolerant to water deprivation conditions in soil-based droughtassays than wild-type plants (Table 12), and one of the lines tested wassignificantly more drought tolerant than the wild-type controls.

Utilities.

Based on the phenotypes observed in morphological and physiologicalassays, G2992 might have a number of applications.

Given the drought and salt tolerance exhibited by 35S::G2992transformants, the gene and its equivalogs might be used to engineerdrought and salt tolerant crops and trees that can flourish in droughtconditions and salinified soils.

The early flowering exhibited by 35S::G2992 lines, indicates that thegene might be used to manipulate flowering time in commercial species.In particular, G2992 could be applied to accelerate flowering oreliminate any requirements for vernalization. In some instances, afaster cycling time might allow additional harvests of a crop to be madewithin a given growing season. Shortening generation times could alsohelp speed-up breeding programs, particularly in species such as trees,which typically grow for many years before flowering. Conversely, itmight be possible to modify the activity of G2992 (or its equivalogs) todelay flowering in order to achieve an increase in biomass and yield.

Finally, the effects of G2992 overexpression on leaf shape suggest thatthe gene might be used to modify plant architecture.

G2994 (SEQ ID NO: 53 and 54)

G2994 is a paralog of G2999 from Arabidopsis. G2994 and closely-relatedclade member sequences each comprise a conserved ZF-HD proteindimerization domain and a homeo_ZF_HD homeobox domain that are expectedto function in a similar manner in each of these related sequences, thatis, by playing a central role in transcriptional regulation and in theconferring of shared traits.

Experimental Observations.

Almost all of the G2994 overexpressors tested were more ABA insensitivethan wild-type controls in plate-based assays.

Utilities.

Given the ABA insensitivity exhibited by 35S::G2994 transformants, thegene and its equivalogs can be used to engineer osmotic stress anddrought tolerant crops and trees.

G2996 (SEQ ID NO: 57 and 58)

G2996 is a paralog of G2999 from Arabidopsis. G2996 and closely-relatedclade member sequences each comprise a conserved ZF-HD proteindimerization domain and a homeo_ZF_HD homeobox domain that are expectedto function in a similar manner in each of these related sequences, thatis, by playing a central role in transcriptional regulation and in theconferring of shared traits.

Experimental Observations.

Many of the G2996 overexpressors tested were larger on 9.4% sucrose thanwild-type controls in plate-based assays.

Utilities.

Given the sugar sensing phenotype exhibited by 35S::G2996 transformants,the gene and its equivalogs can be used to engineer osmotic stress anddrought tolerant crops and trees.

G2997 (SEQ ID NO: 59 and 60)

G2997 is a paralog of G2999 from Arabidopsis. G2997 and closely-relatedclade member sequences each comprise a conserved ZF-HD proteindimerization domain and a homeo_ZF_HD homeobox domain that are expectedto function in a similar manner in each of these related sequences, thatis, by playing a central role in transcriptional regulation and in theconferring of shared traits.

Experimental Observations.

Almost all of the G2997 overexpressors tested were more ABA insensitivethan wild-type controls in plate-based assays.

Utilities.

Given the ABA insensitivity exhibited by 35S::G2997 transformants, thegene and its equivalogs can be used to engineer osmotic stress anddrought tolerant crops and trees.

G3002 (SEQ ID NO: 67 and 68)

G3002 is a paralog of G2999 from Arabidopsis. Seedlings of G3002overexpressors were generally slightly larger than wild-type controls.G3002 and closely-related clade member sequences each comprise aconserved ZF-HD protein dimerization domain and a homeo_ZF_HD homeoboxdomain that are expected to function in a similar manner in each ofthese related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Observations.

G3002 overexpressors were more heat and cold tolerant than wild-typecontrols in plate-based germination and growth assays.

Utilities.

Given the pattern of abiotic stress tolerance exhibited by 35S::G3002transformants, the gene and its equivalogs can be used to engineer heat,drought and cold tolerant crops and trees.

The G3086 Clade of Transcription Factor Polypeptides G3086 (SEQ ID NO:15 and 16)

G3086 corresponds to gene AT1G51140, annotated by the Arabidopsis GenomeInitiative. No information is available about the function(s) of G3086.G3086 and closely-related clade member sequences each comprise aconserved bHLH DNA-binding and dimerization domain that is expected tofunction in a similar manner in each of these related sequences, thatis, by playing a central role in transcriptional regulation and in theconferring of shared traits.

Experimental Observations.

The function of G3086 was studied using transgenic plants in which thegene was expressed under the control of the 35S promoter. Overexpressionof G3086 in Arabidopsis produced a pronounced acceleration in the onsetof flowering. 35S::G3086 transformants produced visible flower buds 5-7days early (in inductive 24-hour light conditions). Some lines weremarkedly smaller than wild-type controls, although a number of lines atthe seedling stage were slightly larger than wild-type plants at thesame stage.

G3086 overexpressing lines were larger and more tolerant of cold stress;the overexpressors were generally larger than the wild type plants whengrown in cold conditions.

35S::G3086 transformants were also larger and displayed more root growthwhen grown under high salt conditions. G3086 overexpressors were larger,greener, and had more root growth than control plants.

Several G3086 overexpressing lines were more tolerant to desiccation inplate-based assays than wild-type control plants.

These abiotic stress assays suggested that this gene may confer droughttolerance, a supposition confirmed in a soil-based assay in which G3086overexpressing-plants were significantly more tolerant of drought stressthan control plants in soil-based drought assays (Tables 11 and 12).

Utilities.

Based on the phenotypes observed in morphological and physiologicalassays, G3086 and its equivalogs might have a number of utilities.

Given the salt resistance exhibited by 35S::G3086 transformants, thegene or its equivalogs might be used to engineer salt tolerant crops andtrees that can flourish in saline soils, or under drought conditions.

Based on the response of 35S::G3086 lines to cold stress, the gene orits equivalogs might be used to engineer crop plants with increasedtolerance to abiotic stresses such as low temperatures, and may thusimprove the range available for planting of many crop species.

The early flowering displayed by 35S::G3086 transformants indicated thatthe gene or its equivalogs might be used to accelerate the flowering ofcommercial species, or to eliminate any requirements for vernalization.

G3086 equivalogs include, for example, Arabidopsis thaliana SEQ ID NO:26 (G592), SEQ ID NO: 28 (G1134), SEQ ID NO: 38 (G2149), SEQ ID NO: 40(G2555); and SEQ ID NO: 42 (G2766); Oryza sativa (japonicacultivar-group) SEQ ID NO: 168 (G3740), SEQ ID NO: 170 (G3741), SEQ IDNO: 172 (G3742), SEQ ID NO: 174 (G3744), and SEQ ID NO: 176 (G3746);Glycine max SEQ ID NO: 180 (G3763), SEQ ID NO: 182 (G3764), SEQ ID NO:184 (G3765), SEQ ID NO: 186 (G3766), SEQ ID NO: 188 (G3767), SEQ ID NO:190 (G3768), SEQ ID NO: 192 (G3769), SEQ ID NO: 194 (G3771), and SEQ IDNO: 196 (G3772); Zea mays SEQ ID NO: 178 (G3755); and Pinus taeda SEQ IDNO: 197 (G3782).

The G354 Clade of Transcription Factor Polypeptides G354 (SEQ ID NO: 227and 228)

G354 was identified in the sequence of BAC clone F12M12, GenBankaccession number AL355775, released by the Arabidopsis GenomeInitiative. G354 corresponds to ZAT7 (Meissner and Michael (1997) PlantMol. Biol. 33: 615-624). G354 and closely-related clade member sequenceseach comprise a conserved C2H2 zinc finger DNA-binding domain that isexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

The highest level of expression of G354 was observed in rosette leaves,embryos, and siliques. Some expression of G354 was also observed inflowers.

The function of this gene was analyzed using transgenic plants in whichG353 was expressed under the control of the 35S promoter. 35S::G354plants had a reduction in flower pedicel length, and downward pointingsiliques. This phenotype was very similar to that described for thebrevipedicellus (bp) mutant (Koornneef et al. (1983) J. Hered. 74:265-272) and in overexpression of a related gene G353. Othermorphological changes in shoots were also observed in 35S::G354 plants.Many 35S::G354 seedlings had abnormal cotyledons, elongated, thickenedhypocotyls, and short roots. The majority of T1 plants had a veryextreme phenotype, were tiny, and arrested development without forminginflorescences. T1 plants showing more moderate effects had poor seedyield.

Overexpression of G354 in Arabidopsis resulted in seedlings with analtered response to light. In a germination assay conducted in darkness,G354 seedlings failed to show an etiolation response. In some cases thephenotype was severe; overexpression of the transgene resulted inreduced open and greenish cotyledons.

G354 overexpressors were also shown to be tolerant to water deprivationin soil-based drought assays (Tables 11 and 12). Closely relatedparalogs of this gene, G353 and G2839, also showed an osmotic stresstolerance phenotype in a germination assay on media containing highsucrose; one line of 35S::G353 seedlings and several lines of 35S::G2839were greener and had higher germination rates than controls. Thus, G354and its paralogs G353 and G2839 appear to influence osmotic stressresponses.

Utilities.

G354 and its equivalogs can be could be used to increase a plant'stolerance to drought and other osmotic stress, and can be used alterinflorescence structure, which may have value in production of novelornamental plants.

G353 (SEQ ID NO: 259 and 260)

G353 is a paralog of G354 from Arabidopsis. G353 and closely-relatedclade member sequences each comprise a conserved C2H2 DNA-binding zincfinger domain that is expected to function in a similar manner in eachof these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Observations.

Overexpressors of G353 have shown an osmotic stress tolerance phenotypein a germination assay on media containing high sucrose. These resultssuggested that the gene may also confer drought tolerance, an indicationconfirmed in soil-based drought assays. In the latter assays, G353overexpressing Arabidopsis plants were more tolerant to initial waterdeprivation, and after rewatering, exhibited superior recovery thanwild-type controls.

Utilities.

G353 and its equivalogs can be could be used to increase a plant'stolerance to drought and other osmotic stress.

G2839 (SEQ ID NO: 249 and 250)

G2839 is a paralog of G354 from Arabidopsis. G2839 and closely-relatedclade member sequences each comprise a conserved C2H2 DNA-binding zincfinger domain that is expected to function in a similar manner in eachof these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

G2839 (At3g46080) was identified in the sequence of BAC F12M12 (GenBankaccession number AL355775) based on its sequence similarity within theconserved domain to other C2H2 related proteins in Arabidopsis. There isno published or public information about the function of G2839.

Experimental Observations.

The function of G2839 was studied using transgenic plants in which thegene was expressed under the control of the 35S promoter. Few primarytransformants were generated, suggesting that G2839 overexpression canbe lethal. T1 lines displayed stunted growth and development, andyielded very few or zero seeds. Inflorescences were poorly developed. Inone line, flower pedicels were very short and flowers and siliques wereoriented downwards. G2839 overexpressors showed a phenotype in agermination assay on media containing high sucrose: seedlings were greenand had high germination rates. Thus, the gene appeared to influencesugar sensing and/or osmotic stress responses.

G2839 is similar to two other Arabidopsis sequences, G354 and G353.Flower phenotypes in which pedicels were very short and flowers andsiliques were oriented downwards have been described for G353 and G354and are also similar to the brevipedicellus mutant (Koornneef et al.(1983) J. Hered. 74: 265-272; Venglat et al. (2002) Proc. Natl. Acad.Sci. USA. 99:4730-4735; Douglas et al. (2002) Plant Cell. 14:547-558.Interestingly 35S::G353 lines also showed increased resistance toosmotic stress.

Supplementing the results of the high sucrose germination assay, G2839was shown to be more tolerant to water deprivation than wild-typecontrol plants in soil-based drought assays (Tables 11 and 12).

Utilities.

The phenotypes observed in physiology assays indicate that G2839 mightbe used to generate crop plants with altered sugar sensing. Since thegene appears to be associated with the response to osmotic stress, thegene could be used to engineer cold and dehydration tolerance. Thelatter was confirmed by the soil-based drought assay.

The morphological phenotype shown by 35S::G2839 lines indicate that thegene might be used to alter inflorescence architecture. In particular, areduction in pedicel length and a change in the position at whichflowers and fruits are held, might influence harvesting or pollinationefficiency. Additionally, such changes might produce attractive novelforms for the ornamental markets.

The G1792 Clade of Transcription Factor Polypeptides G1792 (SEQ ID NO: 7and 8)

G1792 was identified in the sequence of BAC clone K14B15 (AB025608, geneK14B15.14). G1792 and closely-related clade member sequences eachcomprise a conserved AP2 DNA-binding domain that is expected to functionin a similar manner in each of these related sequences, that is, byplaying a central role in transcriptional regulation and in theconferring of shared traits.

Experimental Observations.

G1792 was studied using transgenic plants in which the gene wasexpressed under the control of the 35S promoter.

In soil-based assays, G1792 overexpressing plants were significantlymore drought tolerant than wild-type control plants; 35S::G1792 linesfared much better after a period of water deprivation than controlplants. This distinction was particularly evident in the overexpressorplants when the drought period was followed by rewatering; theoverexpressor plants recovered to a healthy and vigorous state.Conversely, none of the wild-type plants in these experiments recoveredafter rewatering

35S::G1792 plants were more tolerant to the fungal pathogens Fusariumoxysporum and Botrytis cinerea and showed fewer symptoms afterinoculation with a low dose of each pathogen. This result was confirmedusing individual T2 lines. The effect of G1792 overexpression inincreasing tolerance to pathogens received further, incidentalconfirmation. T2 plants of two 35S::G1792 lines had been growing in aroom that suffered a serious powdery mildew infection. For each line, apot of six plants was present in a flat containing nine other pots oflines from unrelated genes. In either of the two different flats, theonly plants that were free from infection were those from the 35S::G1792line. This observation suggested that G1792 overexpression might be usedto increase resistance to powdery mildew. Additional experimentsconfirmed that 35S::G1792 plants showed increased tolerance to Erysiphe.G1792 was ubiquitously expressed, but appeared to be induced bysalicylic acid.

35S::G1792 overexpressing plants also showed more tolerance to growthunder nitrogen-limiting conditions. In a root growth assay underconditions of limiting N, 35S::G1792 lines were slightly less stunted.The lack of anthocyanin production by 35S::G1274 seedlings grown on lownitrogen media supplemented with sucrose plus glutamine, as compared towild-type seedlings which accumulated significant anthocyanin, indicatedthat these lines were less stressed than control seedlings under thesame conditions. These results indicate that G1792 can be involved inmonitoring carbon and nitrogen status in plants.

G1792 overexpressors and wild-type plants were also compared in a coldgermination assay, in which the overexpressors were found to begenerally larger and greener than the controls.

G1792 overexpressing plants showed several mild morphologicalalterations: leaves were dark green and shiny, and plants bolted,subsequently senesced, slightly later than wild-type controls. Among theT1 plants, additional morphological variation (not reproduced later inthe T2 plants) was observed: many showed reductions in size as well asaberrations in leaf shape, phyllotaxy, and flower development.

Utilities.

G1792 or its equivalogs can be used to improve drought and other osmoticstress tolerances, and engineer pathogen-resistant plants. In addition,it can also be used to improve seedling germination and performanceunder conditions of limited nitrogen.

Potential utilities of this gene or its equivalogs also includeincreasing chlorophyll content allowing more growth and productivity inconditions of low light. With a potentially higher photosynthetic rate,fruits could have higher sugar content. Increased carotenoid contentcould be used as a nutraceutical to produce foods with greaterantioxidant capability.

G1792 or its equivalogs could be used to manipulate wax composition,amount, or distribution, which in turn could modify plant tolerance todrought and/or low humidity or resistance to insects, as well as plantappearance (shiny leaves). Increased wax deposition on leaves of a plantlike cotton may improve drought resistance or water use efficiency. Apossible application for this gene might be in reducing the wax coatingon sunflower seeds (the wax fouls the oil extraction system duringsunflower seed processing for oil). For this purpose, antisense orco-suppression of the gene in a tissue-specific manner might be useful

G1792 equivalogs include, for example, Arabidopsis thaliana SEQ ID NO:18 (G30), SEQ ID NO: 34 (G1791), and SEQ ID NO: 36 (G1795); Medicagotruncatula SEQ ID NO: 160 (G3735); Glycine max SEQ ID NO: 82 (G3518),SEQ ID NO: 84 (G3519), SEQ ID NO: 86 (G3520); Oryza sativa (japonicacultivar-group) SEQ ID NO: 70 (G3380), SEQ ID NO: 72 (G3381), SEQ ID NO:74 (G3383), SEQ ID NO: 76 (G3515), and SEQ ID NO: 164 (G3737); Zeamays), SEQ ID NO: 78 (G3516), SEQ ID NO: 80 (G3517), SEQ ID NO: 200(G3794), SEQ ID NO: 166 (G3739) and Triticum aestivum SEQ ID NO: 162(G3736).

G3381 (SEQ ID NO: 71 and 72)

G3381 is a rice ortholog of G1792. G3381 and closely-related clademember sequences each comprise a conserved AP2 DNA-binding domain thatis expected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

In plate-based assays, G3381 overexpressors were more tolerant tomannitol and cold conditions than wild-type controls.

Utilities.

G3381 and its equivalogs may be used to confer osmotic stress, droughtand cold tolerance in plants.

G3383 (SEQ ID NO: 73 and 74) G3383 is a rice ortholog of G1792. G3383and closely-related clade member sequences each comprise a conserved AP2DNA-binding domain that is expected to function in a similar manner ineach of these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Observations.

In plate-based assays, G3383 overexpressors were more tolerant tomannitol, cold and desiccation conditions than wild-type controls.

Utilities.

G3383 and its equivalogs may be used to confer osmotic stress, droughtand cold tolerance in plants.

G3517 (SEQ ID NO: 73 and 74)

G3517 is a corn ortholog of G1792. G3517 and closely-related clademember sequences each comprise a conserved AP2 DNA-binding domain thatis expected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

In plate-based assays, G3517 overexpressors were more tolerant to heat,cold and desiccation conditions than wild-type controls.

Utilities.

G3517 and its equivalogs may be used to confer heat stress, osmoticstress, drought and cold tolerance in plants.

The G2053 Clade of Transcription Factor Polypeptides G2053 (SEQ ID NO: 9and 10)

G2053 was identified in the sequence of BAC T27C4, GenBank accessionnumber AC022287, released by the Arabidopsis Genome Initiative. G2053and closely-related clade member sequences each comprise a conserved NACDNA-binding and dimerization domain that is expected to function in asimilar manner in each of these related sequences, that is, by playing acentral role in transcriptional regulation and in the conferring ofshared traits.

Experimental Observations.

The function of G2053 was analyzed using transgenic plants in which thegene was expressed under the control of the 35S promoter. Overexpressionof G2053 in Arabidopsis resulted in plants with altered osmotic stresstolerance. In a root growth assay on media containing highconcentrations of PEG, G2053 overexpressors showed more root growth andwere generally larger than wild-type controls.

The osmotic stress tolerance assays suggested that this gene may conferdrought tolerance, a supposition confirmed in soil-based assays in whichG2053 overexpressors were significantly more drought tolerant thanwild-type control plants (Tables 11 and 12).

Utilities.

Based on the altered stress tolerance induced by G2053 overexpression,this transcription factor or its equivalogs could be used to alter aplant's response water deficit conditions and, therefore, could be usedto engineer plants with enhanced tolerance to drought, salt stress, andfreezing.

G2053 equivalogs include, for example, Arabidopsis thaliana SEQ ID NO:20 (G515), SEQ ID NO: 22 (G516), and SEQ ID NO: 24 (G517)

G516 (SEQ ID NO: 21 and 22)

G516 is a paralog of G2053 from Arabidopsis. G516 and closely-relatedclade member sequences each comprise a conserved NAC DNA-binding anddimerization domain that is expected to function in a similar manner ineach of these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Observations.

35S::G516 overexpressors were more tolerant to mannitol and cold thanwild-type control plants.

Utilities.

Based on the abiotic assay stress results, G516 could be used toengineer plants with enhanced tolerance to osmotic stress, drought andcold.

The G975 Clade of Transcription Factor Polypeptides G975 (SEQ ID NO: 237and 238)

After its discovery by us, G975 has appeared in the sequences releasedby the Arabidopsis Genome Initiative (BAC F9L1, GenBank accession numberAC007591). G975 and closely-related clade member sequences each comprisea conserved AP2 DNA binding domain that is expected to function in asimilar manner in each of these related sequences, that is, by playing acentral role in transcriptional regulation and in the conferring ofshared traits. G975 and closely-related clade member sequences eachcomprise a conserved AP2 DNA-binding domain that is expected to functionin a similar manner in each of these related sequences, that is, byplaying a central role in transcriptional regulation and in theconferring of shared traits.

Experimental Observations.

G975 was discovered by us and is a new member of the AP2/EREBP family(EREBP subfamily) of transcription factors. G975 is expressed in flowersand, at lower levels, in shoots, leaves, and siliques. GC-FID and GC-MSanalyses of leaves from G975 overexpressing plants have shown that thelevels of C29, C31, and C33 alkanes were substantially increased (up to10-fold) compared to control plants. A number of additional compounds ofsimilar molecular weight, presumably also wax components, alsoaccumulated to significantly higher levels in G975 overexpressingplants. Although total amounts of wax in G975 overexpressing plants havenot yet been measured, C29 alkanes constitute close to 50% of the waxcontent in wild-type plants (Millar et al. (1998) Plant Cell 11:1889-1902), indicating that a major increase in total wax content occursin these transgenic plants. However, the transgenic plants had an almostnormal phenotype (small morphological differences are detected in leafappearance), indicating that overexpression of G975 is not deleteriousto the plant. It is noteworthy that overexpression of G975 did not causethe dramatic alterations in plant morphology that have been reported forArabidopsis plants in which the FATTY ACID ELONGATION1 gene wasoverexpressed (Millar et al. (1998) supra). G975 could specificallyregulate the expression of some of the genes involved in wax metabolism.One Arabidopsis AP2 gene was found that is significantly more closelyrelated to G975 than the rest of the members of the AP2/EREBP family.This other gene, G1387, may have a function, and therefore a utility,related to that of G975.

Plants overexpressing G975 were significantly larger and greener thanwild-type control plants in a soil-based drought assay (Tables 11 and12).

Utilities.

G975 or its equivalogs could be used to improve a plant's tolerance todrought or low water conditions.

G975 or its equivalogs could be used to manipulate wax composition,amount, or distribution, which in turn could modify plant tolerance todrought and/or low humidity or resistance to insects, as well as plantappearance (shiny leaves). A possible application for this gene or itsequivalogs might be in reducing the wax coating on sunflower seeds (thewax fouls the oil extraction system during sunflower seed processing foroil). For this purpose, antisense or co-suppression of the gene in atissue-specific manner might be useful.

G975 could also be used to specifically alter wax composition, amount,or distribution in those plants and crops from which wax is a valuableproduct.

The G1073 Clade of Transcription Factor Polypeptides G1073 (SEQ ID NO:239 and 240), AtHRC1

G1073 has been identified in the sequence of a BAC clone from chromosome4 (BAC clone F23E12, gene F23E12.50, GenBank accession number AL022604),released by EU Arabidopsis Sequencing Project. G1073 and closely-relatedclade member sequences each comprise a conserved At-hook domain and asecond conserved domain (amino acids 43-187) or the DUF296 domain (aminoacids 61-180) that are expected to function in a similar manner in eachof these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Observations.

The function of G1073 was analyzed using transgenic plants in whichG1073 was expressed under the control of the cauliflower mosaic virus35S promoter (these transgenic plants are referred to as “35S::G1073”).Transgenic plants overexpressing G1073 were substantially larger thanwild-type controls, with at least a 60% increase in biomass (Table 10).The increased mass of 35S::G1073 transgenic plants was attributed toenlargement of multiple organ types including stems, roots and floralorgans; other than the size differences, these organs were not affectedin their overall morphology. 35S::G1073 plants exhibited an increase ofthe width (but not length) of mature leaf organs, produced 2-3 morerosette leaves, and had enlarged cauline leaves in comparison tocorresponding wild-type leaves. Overexpression of G1073 resulted in anincrease in both leaf mass and leaf area per plant, and leaf morphology(G1073 overexpressors tended to produce more serrated leaves). We alsofound that root mass was increased in the transgenic plants, and thatfloral organs were also enlarged. An increase of approximately 40% instem diameter was observed in the transgenic plants. Images from thestem cross-sections of 35S::G1073 plants revealed that cortical cellsare large and that vascular bundles contained more cells in the phloemand xylem relative to wild type. Petal size in the 35S::G1073 lines wasincreased by 40-50% compared to wild type controls. Petal epidermalcells in those same lines were approximately 25-30% larger than those ofthe control plants. Furthermore, 15-20% more epidermal cells per petalwere produced compared to wild type. Thus, in petals and stems, theincrease in size was associated with an increase in cell size as well asin cell number.

Seed yield was also increased compared to control plants. 35S::G1073lines showed an increase of at least 70% in seed yield (Table 10). Thisincreased seed production was associated with an increased number ofsiliques per plant, rather than seeds per silique.

TABLE 10 Comparison of biomass and seed yield production in Arabidopsiswild-type and two 35S::G1073 overexpressing lines Line Fresh Weight (g)Dry Weight (g) Seed (g) Wild-type 3.43 ± 0.70 0.73 ± 0.20 0.17 ± 0.0735S::G1073-3 5.74 ± 1.74 1.17 ± 0.30 0.31 ± 0.08 35S::G1073-4 6.54 ±2.19 1.38 ± 0.44 0.35 ± 0.12

All 35S::G1073 lines tested (10/10) exhibited significantly improvedsalt tolerance. Most of these lines also showed a sugar sensingphenotype, exhibiting improved germination on high sucrose media. Oneline showed increased heat germination tolerance. Flowering of G1073overexpressing plants was delayed. Leaves of G1073 overexpressing plantswere generally more serrated than those of wild-type plants. Improveddrought tolerance was observed in 35S::G1073 transgenic lines.

A number of the CUT1::G1073 lines tested exhibited significantlyimproved salt tolerance and sugar sensing on high sucrose. One lineshowed improved germination on high mannitol.

Half of the ARSK::G1073 lines tested ( 5/10) showed improved germinationon high salt, and two lines showed improved germination in cold relativeto controls.

Utilities.

Large size and late flowering produced as a result of G1073 or equivalogoverexpression would be extremely useful in crops where the vegetativeportion of the plant is the marketable portion (often vegetative growthstops when plants make the transition to flowering). In this case, itwould be advantageous to prevent or delay flowering with the use of thisgene or its equivalogs in order to increase yield (biomass). Preventionof flowering by this gene or its equivalogs would be useful in thesesame crops in order to prevent the spread of transgenic pollen and/or toprevent seed set. This gene or its equivalogs could also be used tomanipulate leaf shape, abiotic stress tolerance, including drought andsalt tolerance, and seed yield.

G1069 (SEQ ID NO: 239 and 240)

G1069 is a sequence functionally and structurally related to G1073 fromArabidopsis. G1069 and closely-related clade member sequences eachcomprise a conserved At-hook domain and a second conserved domain (aminoacids 76-218) or the DUF296 domain (amino acids 93-211) that areexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

The sequence of G1069 was obtained from EU Arabidopsis sequencingproject, GenBank accession number Z97336, based on its sequencesimilarity within the conserved domain to other AT-Hook related proteinsin Arabidopsis.

Experimental Observations.

The sequence of G1069 was experimentally determined and the function ofG1069 was analyzed using transgenic plants in which G1069 was expressedunder the control of the 35S promoter.

Plants overexpressing G1069 showed changes in leaf architecture, reducedoverall plant size, and retarded progression through the life cycle.This is a common phenomenon for most transgenic plants in which AT-HOOKproteins are overexpressed if the gene is predominantly expressed inroot in the wild-type background. G1069 was predominantly expressed inroots, based on analysis of RT-PCR results. To minimize thesedetrimental effects, G1069 may be overexpressed under a tissue-specificpromoter such as root- or leaf-specific promoter or under induciblepromoter.

One of G1069 overexpressing lines showed more tolerance to osmoticstress when they were germinated in high sucrose plates. This line alsoshowed insensitivity to ABA in a germination assay.

The high sucrose and ABA assay results suggested that this gene mayconfer increased tolerance to other abiotic stresses when G1069 isoverexpressed. This was subsequently confirmed in soil-based droughtassays in which 35S::G1069 plants were more drought tolerant thanwild-type control plants (Tables 11 and 12).

Utilities.

The drought and osmotic stress results indicate that G1069 could be usedto alter a plant's response to water deficit conditions and, therefore,the gene or its equivalogs could be used to engineer plants withenhanced tolerance to drought, salt stress, and freezing.

G1069 affects ABA sensitivity, and thus when transformed into a plantthe gene or its equivalogs may diminish cold, drought, oxidative andother stress sensitivities, and also be used to alter plantarchitecture, and yield.

G2789 (SEQ ID NO: 247 and 248)

G2789 is a sequence functionally and structurally related to G1073 fromArabidopsis. G2789 and closely-related clade member sequences eachcomprise a conserved At-hook domain and a second conserved domain (aminoacids 68-208) or the DUF296 domain (amino acids 86-201) that areexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

The sequence of G2789 was obtained from Arabidopsis genomic sequencingproject, GenBank accession number AL162295, based on its sequencesimilarity within the conserved domain to other AT-hook related proteinsin Arabidopsis. G2789 corresponds to gene T4C21_280 (CAB82691). To date,there is no published information regarding the functions of this gene.

Experimental Observations.

The complete sequence of G2789 was determined. G2789 is expressed atmoderate levels in roots, flowers, embryos, siliques, and germinatingseeds. It was not detectable in rosette leaves or shoots. No significantinduction of G2789 was observed in rosette leaves by any conditiontested.

The function of this gene was analyzed using transgenic plants in whichG2789 was expressed under the control of the 35S promoter.Overexpression of G2789 in Arabidopsis resulted in seedlings that areABA insensitive and osmotic stress tolerant. In a germination assay onABA containing media, G2789 transgenic seedlings showed enhancedseedling vigor. In a similar germination assay on media containing highconcentrations of sucrose, the G2789 overexpressors also showed enhancedseedling vigor. In a repeat experiment on individual lines, all threelines show the phenotype. The combination of ABA insensitivity andbetter germination under osmotic stress was also observed for G1820. Itis possible that ABA insensitivity at the germination stage promotesgermination despite unfavorable conditions.

The osmotic stress tolerance and enhanced seedling vigor on ABAphenotypes suggested that G2789 overexpressors would be more tolerant todrought conditions This supposition was confirmed by soil-based droughtassays, in which plants overexpressing G2789 performed significantlybetter in conditions of water deprivation than wild-type plants (Tables11 and 12).

Utilities.

G2789 could be used to alter a plant's response to water deficitconditions and therefore, could be used to engineer plants with enhancedtolerance to drought, salt stress, and freezing.

Rice G3399 (SEQ ID NO: 339 and 340)

G3399 is a rice ortholog of G1073. Phylogenetic analysis identifiesG3399 along with G3400 as being the most closely related rice orthologsof G1073. G3399 and closely-related clade member sequences each comprisea conserved At-hook domain and a second conserved domain (amino acids108-253) or the DUF296 domain (amino acids 126-246) that are expected tofunction in a similar manner in each of these related sequences, thatis, by playing a central role in transcriptional regulation and in theconferring of shared traits.

The morphologically similar effects caused by overexpression of thisrice gene versus G1073 and other Arabidopsis paralogs suggest that theylikely have related functions. A number of Arabidopsis linesoverexpressing G3399 and G3407 under the control of the 35S promoterwere found be larger, with broader leaves and larger rosettes thanwild-type control plants. Two of the lines overexpressing G3399 werefound to have greater tolerance to desiccation and heat than wild-typecontrols in plate-based assays, and drought in soil-based assays.

Utilities.

G3399 could be used to increase a plant's biomass and alter a plant'sresponse to cold and water deficit conditions and, therefore, could beused to engineer plants with enhanced tolerance to drought.

Rice G3407 (SEQ ID NO: 353 and 354)

G3407 is a rice ortholog of G1073. G3407 and closely-related clademember sequences each comprise a conserved At-hook domain and a secondconserved domain (amino acids 72-220) or the DUF296 domain (amino acids90-213) that are expected to function in a similar manner in each ofthese related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

The morphologically similar effects caused by overexpression of thisrice gene versus G1073 and other Arabidopsis paralogs suggest that theylikely have related functions.

Experimental Observations.

At the seedling stage, about half of the 35S::G3407 lines appearedlarger than controls. At later stages of growth, lines overexpressingG3407 showed no consistent morphological differences from controlplants, with the exception of one line which was 50% larger thancontrols at the rosette stage.

Two lines of overexpressors were less sensitive germination in coldconditions than wild type controls.

Utilities.

G3407 could be used to increase a plant's biomass and engineer plantswith enhanced tolerance to cold.

Soybean G3456 (SEQ ID NO: 383 and 384)

G3456 is a sequence functionally and structurally related to G1073 fromArabidopsis. G3456 and closely-related clade member sequences eachcomprise a conserved At-hook domain and a second conserved domain (aminoacids 53-195) or the DUF296 domain (amino acids 71-188) that areexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

A significant number of Arabidopsis lines overexpressing G3456 under thecontrol of the 35S promoter were found be larger, with broader leavesand larger rosettes than wild-type control plants.

Most of the lines overexpressing G3456 were significantly more coldtolerant than wild-type controls. Several 35S::G3456 lines were found tohave greater salt tolerance than wild type controls. Several lines ofoverexpressors were much more tolerant to drought than wild-typecontrols in soil-based assays.

Utilities.

G3456 can be used to increase a plant's biomass. G3456 may be also usedto alter a plant's response to water deficit conditions and, therefore,could be used to engineer plants with enhanced tolerance to drought andsalt stress.

Soybean G3459 (SEQ ID NO: 387 and 388)

G3459 is a sequence functionally and structurally related to G1073 fromArabidopsis. G3459 and closely-related clade member sequences eachcomprise a conserved At-hook domain and a second conserved domain (aminoacids 86-228) or the DUF296 domain (amino acids 104-221) that areexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

A significant number of Arabidopsis lines overexpressing G3459 under thecontrol of the 35S promoter were found be larger, with broader leavesand larger rosettes than wild-type control plants.

Most of the lines overexpressing G3459 conferred tolerance to oneabiotic stress, and were significantly more salt, heat or cold tolerantthan wild-type controls.

Utilities.

G3459 can be used to increase a plant's biomass. G3459 may be also usedto alter a plant's response to water deficit conditions and, therefore,could be used to engineer plants with enhanced tolerance to salt, heat,cold and drought.

Soybean G3460 (SEQ ID NO: 389 and 390)

G3460 is a sequence functionally and structurally related to G1073 fromArabidopsis. G3460 and closely-related clade member sequences eachcomprise a conserved At-hook domain and a second conserved domain (aminoacids 83-225) or the DUF296 domain (amino acids 101-218) that areexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

A significant number of Arabidopsis lines overexpressing G3460 under thecontrol of the 35S promoter were found be larger, with broader leavesand larger rosettes than wild-type control plants.

Most of the lines overexpressing G3459 conferred tolerance to oneabiotic stress, and were significantly more heat, desiccation or coldtolerant than wild-type controls. Several lines of overexpressors weremuch more tolerant to drought than wild-type controls in soil-basedassays.

Utilities.

G3460 can be used to increase a plant's biomass.

G3460 may be also used to alter a plant's response to water deficitconditions and, therefore, could be used to engineer plants withenhanced tolerance to heat, drought, and cold.

The G482 Clade of Transcription Factor Polypeptides G481 (PolynucleotideSEQ ID NO: 287 and 288)

G481 is equivalent to AtHAP3a which was identified by Edwards et al.,((1998) Plant Physiol. 117: 1015-1022) as an EST with extensive sequencehomology to the yeast HAP3. G481 is a member of the HAP3 subgroup of theCCAAT box-binding transcription factor family. G481 and closely-relatedclade member sequences each a conserved CCAAT box-binding domain that isexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

Northern blot data from five different tissue samples indicates thatG481 is primarily expressed in flower and/or silique, and root tissue.The function of G481 was analyzed through its ectopic overexpression inplants. Except for darker color in one line (noted below), plantsoverexpressing G481 had a wild-type morphology. G481 overexpressors werefound to be more tolerant to high sucrose and high salt, having bettergermination, longer radicles, and more cotyledon expansion. There was aconsistent difference in the hypocotyl and root elongation in theoverexpressor compared to wild-type controls. These results indicatedthat G481 is involved in sucrose-specific sugar sensing. Sucrose-sensinghas been implicated in the regulation of source-sink relationships inplants.

In the T2 generation, one overexpressing line was darker green thanwild-type plants, which may indicate a higher photosynthetic rate thatwould be consistent with the role of G481 in sugar sensing.

35S::G481 plants were also significantly larger and greener in asoil-based drought assay than wild-type controls plants After eight daysof drought treatment overexpressing lines had a darker green and lesswithered appearance than those in the control group. The differences inappearance between the control and G481-overexpressing plants after theywere rewatered was even more striking. Eleven of twelve plants of thisset of control plants died after rewatering, indicating the inability torecover following severe water deprivation, whereas all nine of theoverexpressor plants of the line shown recovered from this droughttreatment. These results were typical of a number of control and35S::G481-overexpressing lines.

One line of plants in which G481 was overexpressed under the control ofthe ARSK1 root-specific promoter was found to germinate better undercold conditions than wild-type plants.

Interestingly, in one Arabidopsis line in which G481 was knocked out,the plants were found to be more sensitive to high salt in a plate-basedassay than wild-type plants, which indicates the importance of the roleplayed by G481 in regulating osmotic stress tolerance, and demonstratesthat the gene is both necessary and sufficient to fulfill that function.

A number of the 35S::G481 plants evaluated had a late floweringphenotype.

Utilities.

The potential utility of G481 includes altering photosynthetic rate,which could also impact yield in vegetative tissues as well as seed.Sugars are key regulatory molecules that affect diverse processes inhigher plants including germination, growth, flowering, senescence,sugar metabolism and photosynthesis. Sucrose is the major transport formof photosynthate and its flux through cells has been shown to affectgene expression and alter storage compound accumulation in seeds(source-sink relationships).

Since G481 overexpressing plants performed better than controls indrought experiments, this gene or its equivalogs may be used to improveseedling vigor, plant survival, as well as yield, quality, and range.

G482 (Polynucleotide SEQ ID NO: 289 and 290)

G482, a paralog of G481, is equivalent to AtHAP3b which was identifiedby Edwards et al. (1998) Plant Physiol. 117: 1015-1022) as an EST withhomology to the yeast gene HAP3b. Their northern blot data suggests thatAtHAP3b is expressed primarily in roots. G482 is a member of the HAP3subgroup of the CCAAT box-binding transcription factor family. G482 andclosely-related clade member sequences each a conserved CCAATbox-binding domain that is expected to function in a similar manner ineach of these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR analysis of endogenous levels of G482 transcripts indicated thatthis gene is expressed constitutively in all tissues tested. A cDNAarray experiment supports the RT-PCR derived tissue distribution data.G482 is not induced above basal levels in response to any environmentalstress treatments tested.

A T-DNA insertion mutant for G482 was analyzed and was found to flowerslightly later than control plants.

The function of G482 was also analyzed through its ectopicoverexpression in plants. Plants overexpressing G482 had a wild-typemorphology. Germination assays to measure salt tolerance demonstratedincreased seedling growth when germinated on the high salt medium.

35S::G482 transgenic plants also displayed an osmotic stress responsephenotype similar to 35S::G481 transgenic lines. Five of tenoverexpressing lines had increased seedling growth on medium containing80% MS plus vitamins with 300 mM mannitol.

Three of ten 35S::G482 lines also demonstrated enhanced germinationrelative to controls after a 6 hour exposure to 32° C.

The majority of these 35S::G482 lines also demonstrated a slightly earlyflowering phenotype.

Utilities.

The potential utilities of this gene include the ability to conferosmotic stress tolerance, as measured by salt, heat tolerance andimproved germination in mannitol-containing media, during thegermination stage of a crop plant. This would most likely impactsurvivability and yield. Evaporation of water from the soil surfacecauses upward water movement and salt accumulation in the upper soillayer, where the seeds are placed. Thus, germination normally takesplace at a salt concentration much higher than the mean saltconcentration in the whole soil profile.

Improved osmotic stress tolerance is also likely to result in enhancedseedling vigor, plant survival, improved yield, quality, and range.Osmotic stress assays, including subjecting plants to aqueous dissolvedsugars, are often used as surrogate assays for improved water-stress(for example, drought) response. Thus, G482 may also be used to improveplant performance under conditions of water deprivation, includingincreased seedling vigor, plant survival, yield, quality, and range.

Rice G3395 (SEQ ID NO: 331 and 332)

G3395 (rice) is an ortholog of G481 and G482, and is a member of theHAP3-like subfamily of CCAAT-box binding transcription factors. G3395corresponds to polypeptide BAC76331 (“NF-YB subunit of rice”). G3395 andclosely-related clade member sequences each a conserved CCAATbox-binding domain that is expected to function in a similar manner ineach of these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Observations.

The function of G3395 was analyzed through its ectopic overexpression inplants. One of the lines of 35S::G3395 overexpressors tested was foundto be more tolerant to high salt levels, producing larger and greenerseedlings in a high salt germination assay. Several lines were alsosignificantly more drought tolerant than wild type controls insoil-based assays.

Utilities.

The potential utilities of G3395 include the ability to confer salt anddrought stress tolerance

Soy G3470 (SEQ ID NO: 393 and 394)

G3470 (soybean) is an ortholog of G481 and G482, and is a member of theHAP3-like subfamily of CCAAT-box binding transcription factors. G3470and closely-related clade member sequences each a conserved CCAATbox-binding domain that is expected to function in a similar manner ineach of these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Observations.

The function of G3470 was analyzed through its ectopic overexpression inplants. Seven of ten lines of 35S::G3470 overexpressors were found to besignificantly more tolerant to high salt in a plate-based germinationassay.

Utilities.

The potential utilities of these two genes, G3395 and G3470, and theirequivalogs, include the ability to confer tolerance to drought and otherosmotic stresses, including during the germination stage of a cropplant. Equivalogs of G3395 and G3470 include, for example, Arabidopsissequences G481 (SEQ ID NO: 288), G482 (SEQ ID NO: 290), G485 (SEQ ID NO:292), G486 (SEQ ID NO: 294), G1248 (SEQ ID NO: 306), G1364 (SEQ ID NO:308), G1781 (SEQ ID NO: 310), G2345 (SEQ ID NO: 320), G2718 (SEQ ID NO:324), rice sequences G3394 (SEQ ID NO: 330), G3396 (SEQ ID NO: 334),G3397 (SEQ ID NO: 336), G3398 (SEQ ID NO: 338), G3429 (SEQ ID NO: 358),G3835 (SEQ ID NO: 414), G3836 (SEQ ID NO: 416), corn sequences G3434(SEQ ID NO: 362), G3435 (SEQ ID NO: 364), G3436 (SEQ ID NO: 366), G3437(SEQ ID NO: 368), and soy sequences G3470 (SEQ ID NO: 394), G3471 (SEQID NO: 396), G3472 (SEQ ID NO: 398), G3473 (SEQ ID NO: 400), G3474 (SEQID NO: 402), G3475 (SEQ ID NO: 404), G3476 (SEQ ID NO: 406), G3477 (SEQID NO: 408), G3478 (SEQ ID NO: 410), and G3837 (SEQ ID NO: 418).

HAP5 Transcription Factor Polypeptides G1820 (SEQ ID NO: 243 and 244)

G1820 is a member of the Hap5 subfamily of CCAAT-box-bindingtranscription factors. G1820 was identified as part of the BAC cloneMBA10, accession number AB025619 released by the Arabidopsis Genomesequencing project. G1820 and closely-related clade member sequenceseach comprise a conserved CCAAT binding factor domain that is expectedto function in a similar manner in each of these related sequences, thatis, by playing a central role in transcriptional regulation and in theconferring of shared traits.

Experimental Observations.

The complete sequence of G1820 was determined. The function of this genewas analyzed using transgenic plants in which G1820 was expressed underthe control of the 35S promoter. G1820 overexpressing lines showed moretolerance to salt stress in a germination assay. They also showedinsensitivity to ABA, with the three lines analyzed showing thephenotype. The salt and ABA phenotypes could be related to the plants'increased tolerance to osmotic stress, which was subsequently confirmedin soil-based drought assays in which 35S::G1820 plants weresignificantly more drought-tolerant than wild-type control plants(Tables 11 and 12).

Interestingly, overexpression of G1820 also consistently reduced thetime to flowering. Under continuous light conditions at 20-25 C, the35S::G1820 transformants displayed visible flower buds several daysearlier than control plants. The primary shoots of these plantstypically started flower initiation 1-4 leaf plastochrons sooner thanthose of wild type. Such effects were observed in all three T2populations and in a substantial number of primary transformants.

When biochemical assays were performed, some changes in leaf fames weredetected. In one line, an increase in the percentage of 18:3 and adecrease in 16:1 were observed. Otherwise, G1820 overexpressors behavedsimilarly to wild-type controls in all biochemical assays performed. Asdetermined by RT-PCR, G1820 was highly expressed in embryos andsiliques. No expression of G1820 was detected in the other tissuestested. G1820 expression appeared to be induced in rosette leaves bycold and drought stress treatments, and overexpressing lines showedtolerance to water deficit and high salt conditions.

One possible explanation for the complexity of the G1820 overexpressionphenotype is that the gene is somehow involved in the cross talk betweenABA and GA signal transduction pathways. It is well known that seeddormancy and germination are regulated by the plant hormones ABA andgibberellin (GA). These two hormones act antagonistically with eachother. ABA induces seed dormancy in maturing embryos and inhibitsgermination of seeds. GA breaks seed dormancy and promotes germination.It is conceivable that the flowering time and ABA insensitive phenotypesobserved in the G1820 overexpressors are related to an enhancedsensitivity to GA, or an increase in the level of GA, and that thephenotype of the overexpressors is unrelated to ABA. In Arabidopsis, GAis thought to be required to promote flowering in non-inductivephotoperiods. However, the drought and salt tolerant phenotypes wouldindicate that ABA signal transduction is also perturbed in these plants.It seems counterintuitive for a plant with salt and drought tolerance tobe ABA insensitive since ABA seems to activate signal transductionpathways involved in tolerance to salt and dehydration stresses. Oneexplanation is that ABA levels in the G1820 overexpressors are also highbut that the plant is unable to perceive or transduce the signal.

G1820 overexpressors also had decreased seed oil content and increasedseed protein content compared to wild-type plants

Utilities.

G1820 and its equivalogs may be used to enhance a plant's tolerance todrought conditions. The osmotic stress results indicated that G1820 orits equivalogs could be used to alter a plant's response to additionalwater deficit conditions and can be used to engineer plants withenhanced tolerance to salt stress, and freezing. Evaporation from thesoil surface causes upward water movement and salt accumulation in theupper soil layer where the seeds are placed. Thus, germination normallytakes place at a salt concentration much higher than the mean saltconcentration of in the whole soil profile. Increased salt toleranceduring the germination stage of a crop plant would impact survivabilityand yield.

G1820 affects ABA sensitivity, and thus when transformed into a plantthis transcription factor or its equivalogs may diminish cold, drought,oxidative and other stress sensitivities, and also be used to alterplant architecture, and yield.

G1820 or its equivalogs could also be used to accelerate flowering time.

G1820 or its equivalogs may be used to modify levels of saturation inoils.

G1820 or its equivalogs may be used to seed protein content.

The promoter of G1820 could be used to drive seed-specific geneexpression.

G1820 or equivalog overexpression may be used to alter seed proteincontent, which may be very important for the nutritional value andproduction of various food products

G489 (SEQ ID NO: 229 and 230)

G489 was identified from a BAC sequence that showed high sequencehomology to AtHAP5-like transcription factors in Arabidopsis. G489 andclosely-related clade member sequences each comprise a conserved CCAATbinding factor domain that is expected to function in a similar mannerin each of these related sequences, that is, by playing a central rolein transcriptional regulation and in the conferring of shared traits.

Experimental Observations.

The function of G489 was analyzed through its ectopic overexpression inplants.

RT-PCR analysis of endogenous levels of G489 transcripts indicates thatthis gene is expressed constitutively in all tissues tested. A cDNAarray experiment confirms the RT-PCR derived tissue distribution data.G489 was not induced above basal levels in response to the stresstreatments tested.

G489 overexpressors were more tolerant to high NaCl stress, showing moreroot growth and leaf expansion compared to the controls in culture. Twowell characterized ways in which NaCl toxicity is manifested in theplant is through general osmotic stress and potassium deficiency due tothe inhibition of its transport. These lines were more tolerant toosmotic stress, showing more root growth on mannitol containing media;however, they were not more tolerant to potassium deficiency.

The involvement of G489 in a response pathway to abiotic stress wasfurther confirmed in soil-based drought assays, where the overexpressorswere observed to be more tolerant to water deprivation conditions thanwild-type control plants (Table 12).

Utilities.

The potential utilities of this gene include the ability to conferdrought and salt tolerance during the growth and developmental stages ofa crop plant. This would most likely impact yield and or biomass.

The G916 Clade of Transcription Factor Polypeptides G916 (SEQ ID NO: 235and 236)

G916 corresponds to gene At4g04450, and it has also been described asWRKY42. No information is available about the function(s) of G916. G916and closely-related clade member sequences each comprise a conservedWRKY DNA-binding domain that is expected to function in a similar mannerin each of these related sequences, that is, by playing a central rolein transcriptional regulation and in the conferring of shared traits.

Experimental Observations.

The complete cDNA sequence of G916 was experimentally determined. G916appears to be expressed at low levels in a range of tissues, and was notsignificantly induced by any of the conditions tested.

A T-DNA insertion mutant for G916, displayed wild-type morphology.Overexpression of G916 produced a wide spectrum of developmentalabnormalities in Arabidopsis. Many of the 35S::G916 seedlings wereextremely tiny and showed an apparent lack of shoot organization. Suchplants arrested growth and died at very early stages. Other individualswere small and displayed disproportionately long hypocotyls and narrowcotyledons. At later stages, the majority of surviving lines weremarkedly smaller than wild type, and formed rather weedy inflorescencestems that yielded very few flowers. Additionally, flowers often hadpoorly developed organs.

In addition, G916 overexpressing lines were larger than controlwild-type seedlings in several germination assays. Larger seedlings wereobserved under conditions of high sucrose. In addition, 35S::G916seedlings were larger and appeared to have less anthocyanin on highsucrose plates that were nitrogen deficient, with or without glutaminesupplementation. The assays monitor the effect of C on N signalingthrough anthocyanin production. That 35S::G916 seedlings performedbetter under conditions of high sucrose alone makes it more difficult tointerpret the better seedling performance under conditions of lownitrogen. Tissue-specific or inducible expression of this gene could aidin sorting out the complex phenotypes caused by the constitutiveoverexpression of this gene.

The results of the high sucrose assays indicated thatG916-overexpressing plants might be significantly more drought tolerantthan control plants, which was subsequently confirmed in soil-baseddrought assays (Tables 11 and 12).

Utilities.

The results of physiological assays indicate that G916 could be used toalter the sugar signaling in plants. The soil-based drought and sugarsensing assays indicate that G916 and its equivalogs may also be used toenhance a plant's drought or other osmotic stress tolerance.

The enhanced performance of G916 overexpression lines under low nitrogenconditions indicate that the gene could be used to engineer crops thatcould thrive under conditions of reduced nitrogen availability.

That 35S::G916 lines make less anthocyanin on high sucrose plusglutamine, indicates G916 might be used to modify carbon and nitrogenstatus, and hence assimilate partitioning.

Additionally, the morphological phenotypes shown by 35S::G916 seedlingsindicate that the gene might be used to manipulate light responses suchas shade avoidance.

The G2701 Clade of Transcription Factor Polypeptides G2701 (SEQ ID NO:245 and 246)

G2701 was identified in the sequence of BAC F11B9, GenBank accessionnumber AC073395, released by the Arabidopsis Genome Initiative. G2701and closely-related clade member sequences each comprise at least oneconserved Myb-related DNA-binding domain that is expected to function ina similar manner in each of these related sequences, that is, by playinga central role in transcriptional regulation and in the conferring ofshared traits.

Experimental Observations.

The function of G2701 was analyzed using transgenic plants in which thegene was expressed under the control of the 35S promoter. Overexpressionof G2701 is Arabidopsis resulted in plants that were wild-type inmorphology and in the biochemical analyses performed. However,35S::G2701 transgenic plants were more tolerant to osmotic stress in agermination assay, the seedlings were greener with expanded cotyledonsand longer roots than wild-type controls when germinated on platescontaining either high salt or high sucrose. The phenotype was repeatedin all three lines.

The results of the high sucrose and salt assays suggested that this genewould confer increased tolerance to other abiotic stresses when G2701 isoverexpressed, which was subsequently confirmed in soil-based droughtassays, in which 35S::G2701 plants were significantly more droughttolerant than wild-type control plants (Tables 11 and 12).

G2701 was expressed ubiquitously in Arabidopsis according to RT-PCR, andthe level of G2701 expression in leaf tissue was essentially unchangedin response to environmental stress related conditions.

Utilities.

G2701 or its equivalogs could be used to alter a plant's response towater deficit conditions and therefore, could be used to engineer plantswith enhanced tolerance to drought, salt stress, and freezing.

The G2854 Clade of Transcription Factor Polypeptides G2854 (SEQ ID NO:251 and 256)

The sequence of G2854 was obtained from the Arabidopsis genomesequencing project, GenBank accession number AL161566, nid=7269538,based on its sequence similarity within the conserved domain to otherACBF-like related proteins in Arabidopsis. G2854 and closely-relatedclade member sequences each comprise at least one conserved RNARecognition Motif (RRM; also known as an RBD or RNP domain) that isexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

The 5′ and 3′ ends of G2854 were determined by RACE. The function ofG2854 was analyzed using transgenic plants in which G2854 was expressedunder the control of the 35S promoter. 35S::G2854 transformants showedincreased germination efficiency on sucrose plates compared to wild-typecontrols. These results suggested a possible role for G2854 inconferring drought tolerance in plants. This supposition was confirmedin soil-based drought assays, in which plants overexpressing G2854performed significantly better than wild-type plants (Tables 11 and 12).

Utilities.

G2854 and its equivalogs may be used to confer improved droughttolerance in plants.

G2854 and its equivalogs might also be used to generate crop plants withaltered sugar sensing. Sugars are key regulatory molecules that affectdiverse processes in higher plants including germination, growth,flowering, senescence, sugar metabolism and photosynthesis. Sucrose isthe major transport form of photosynthate and its flux through cells hasbeen shown to affect gene expression and alter storage compoundaccumulation in seeds (source-sink relationships). Glucose-specifichexose-sensing has been described in plants and implicated in celldivision and repression of ‘famine’ genes (photosynthetic or glyoxylatecycles). The potential utilities of a gene involved in glucose-specificsugar sensing are to alter energy balance, photosynthetic rate,carbohydrate accumulation, biomass production, source-sinkrelationships, and senescence.

The G634 Clade of Transcription Factor Polypeptides G634 (SEQ ID NO: 231and 232)

G634 was initially identified as public partial cDNAs sequences for GTL1and GTL2 which are splice variants of the same gene (Small et al (1998)Proc. Natl. Acad. Sci. USA. 95:3318-3322). The published expressionpattern of GTL1 shows that G634 is highly expressed in siliques and notexpressed in leaves, stems, flowers or roots. G634 and closely-relatedclade member sequences each comprise at least one conserved TH domainthat is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

The boundaries of G634 in were experimentally determined and thefunction of G634 was investigated by constitutively expressing G634using the CaMV 35S promoter.

Three constructs were made for G634: P1374, P324, and P1717 (SEQ ID NOs:1013, 1015 and 1017, respectively). P324 was found to encode a truncatedprotein. P1374 and P1717 represent full length splice variants of G634;P1374, the shorter of the two splice variants was used for theexperiments described here. The longest available cDNA (P1717),confirmed by RACE, has the same ATG and stop codons as the genomicsequence.

Plants overexpressing G634 from construct P1374 showed a dramaticincrease the density of trichomes, which additionally appear larger insize. The increase in trichome density was most noticeable on laterarising rosette leaves, cauline leaves, inflorescence stems and sepalswith the stem trichomes being more highly branched than controls.Approximately half of the primary transformants and two of three T2lines showed the phenotype. Apart from slight smallness, there did notappear to be any other clear phenotype associated with theoverexpression of G634. However, a reduction in germination was observedin T2 seeds grown in culture. It is not clear whether this defect wasdue to the quality of the seed lot tested or whether this characteristicis related to the transgene overexpression.

RT PCR data showed that G634 is potentially preferentially expressed inflowers and germinating seedlings, and induced by auxin. The role ofauxin in trichome initiation and development has not been established inthe published literature.

The increase in trichome density observed in G634 overexpressorssuggested a possible role for this gene in drought-stress tolerance, apresumption subsequently confirmed in soil-based drought assays (Tables11 and 12).

Utilities.

Trichome glands on the surface of many higher plants produce and secreteexudates that give protection from the elements and pests such asinsects, microbes and herbivores. These exudates may physicallyimmobilize insects and spores, may be insecticidal or ant-microbial orthey may allergens or irritants to protect against herbivores. Trichomeshave also been suggested to decrease transpiration by decreasing leafsurface air flow, and by exuding chemicals that protect the leaf fromthe sun.

Depending on the plant species, varying amounts of diverse secondarybiochemicals (often lipophilic terpenes) are produced and exuded orvolatilized by trichomes. These exotic secondary biochemicals, which arerelatively easy to extract because they are on the surface of the leaf,have been widely used in such products as flavors and aromas, drugs,pesticides and cosmetics. One class of secondary metabolites, thediterpenes, can effect several biological systems such as tumorprogression, prostaglandin synthesis and tissue inflammation. Inaddition, diterpenes can act as insect pheromones, termite allomones,and can exhibit neurotoxic, cytotoxic and antimitotic activities. As aresult of this functional diversity, diterpenes have been the target ofresearch several pharmaceutical ventures. In most cases where themetabolic pathways are impossible to engineer, increasing trichomedensity or size on leaves may be the only way to increase plantproductivity.

Thus, the use of G634 and its equivalogs to increase trichome density,size or type may therefore have profound utilities in so calledmolecular farming practices (i.e. the use of trichomes as amanufacturing system for complex secondary metabolites), and inproducing resistant insect and herbivore resistant plants.

G634 and its equivalogs may also be used to increase the droughttolerance of plants.

The G175 Clade of Transcription Factor Polypeptides G175 (SEQ ID NO: 223and 224)

G175 was identified in the sequence of P1 clone M3E9 (GeneAT4g26440/M3E9.130; GenBank accession number CAB79499). G175 andclosely-related clade member sequences each comprise a conserved WRKYDNA-binding domain that is expected to function in a similar manner ineach of these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Observations.

The complete cDNA sequence of G175 was determined by us. The function ofthis gene was studied using transgenic plants in which G175 wasexpressed under the control of the 35S promoter. 35S::G175 plants aremore tolerant to osmotic stress conditions (better germination in NaCland sucrose containing media). The plants were otherwise wild-type inmorphology and development.

G175 appears to be specifically expressed in floral tissues, and alsoappears to be induced elsewhere by heat and salt stress.

The results of the osmotic stress assays and heat and salt stressexpression analyses suggested that G175 could be used to confer droughttolerance in plants, a supposition that was confirmed in soil-basedassays in which G175-overexpressing plants were shown to be moretolerant to water deprivation than wild-type control plants (Tables 11and 12).

Utilities.

G175 and its equivalogs can be used to improve drought tolerance andincrease germination under adverse osmotic stress conditions, whichcould impact survivability and yield. The promoter of G175 could also beused to drive flower specific expression.

The G1452 Clade of Transcription Factor Polypeptides G1452 (SEQ ID NO:241 and 242)

G1452 was identified in the sequence of clones T22O13, F12K2 withaccession number AC006233 released by the Arabidopsis Genome Initiative.G1452 and closely-related clade member sequences each comprise aconserved NAC domain that is expected to function in a similar manner ineach of these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Observations.

The function of G1452 was analyzed using transgenic plants in which thegene was expressed under the control of the 35S promoter. G1452 andclosely-related clade member sequences each comprise a conserved NACdomain that is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Overexpression of G1452 produced changes in leaf development andmarkedly delayed the onset of flowering. 35S::G1452 plants produced darkgreen, flat, rounded leaves, and typically formed flower buds between 2and 14 days later than controls. Additionally, some of the transformantswere noted to have rather low trichome density on leaves and stems. Atlater stages of life cycle, 35S::G1452 appeared to develop slowly andsenesced considerably later than wild-type controls.

G1452 overexpressors were more tolerant to high sucrose-induced osmoticstress than wild-type control plants, were more tolerant to high saltthan controls, and were insensitive to ABA in separate germinationassays. These results indicated that G1452 may be used to conferimproved survival in drought, which was confirmed in soil-based droughtassays where G1452-overexpressors fared significantly better thanwild-type control plants (Tables 11 and 12).

Utilities.

G1452 could be used to alter a plant's response to water deficitconditions and therefore, could be used to engineer plants with enhancedtolerance to drought and salt stress.

On the basis of the analyses performed to date, G1452 could be use toalter plant growth and development.

The G3083 Clade of Transcription Factor Polypeptides G3083 (SEQ ID NO:253 and 254)

G3083 (At3g14880) was identified as part of the BAC clone K15M2, GenBankaccession number AP000370 (nid=5541653). G3083 and closely-related clademember sequences each comprise a conserved domain that is expected tofunction in a similar manner in each of these related sequences, thatis, by playing a central role in transcriptional regulation and in theconferring of shared traits.

Experimental Observations.

The 5′- and 3′-ends of G3083 were determined by RACE and the function ofthe gene was assessed by analysis of transgenic Arabidopsis lines inwhich a genomic clone was constitutively expressed from a 35S promoter.35S::G3083 plants were indistinguishable from wild-type controls in themorphological analysis.

In the physiological analysis, two out of the three 35S::G3083 linestested, displayed an enhanced ability to germinate on plates containinghigh levels of sodium chloride. This suggested that G3083 might functionas part of a response pathway to abiotic stress, which was furtherindicated in soil-based drought assays in which one line of a G3083overexpressor was shown to be significantly more tolerant to waterdeprivation than wild-type control plants.

Utilities

Based on the increased salt tolerance exhibited by the 35S::G3083 linesin physiology assays, this gene might be used to engineer salt tolerantcrops and trees that can flourish in drought or in salinified soils. Thelatter condition is of particular importance early in the lifecycle,since evaporation from the soil surface causes upward water movement,and salt accumulates in the upper soil layer where the seeds are placed.Thus, germination normally takes place at a salt concentration muchhigher than the mean salt level in the whole soil profile. Increasedsalt tolerance during the germination stage of a crop plant wouldtherefore enhance survivability and yield.

The G303 Clade of Transcription Factor Polypeptides G303 (SEQ ID NO: 225and 226)

G303 corresponds to gene MNA5.5 (BAB11554.1). G303 and closely-relatedclade member sequences each comprise a conserved HLH DNA-binding anddimerization domain that is expected to function in a similar manner ineach of these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Observations.

The complete sequence of G303 was determined. G303 was detected at verylow levels in roots and rosette leaves. It did not appear to be inducedby any condition tested. No altered morphological or biochemicalphenotypes were detected in G303 overexpressing plants.

The function of this gene was analyzed using transgenic plants in whichG303 was expressed under the control of the 35S promoter. G303overexpressing plants showed more tolerance to osmotic stress vigor thanwild-type controls in a germination assay in three separate experimentson high salt and high sucrose.

The involvement of G303 in a response pathway to abiotic stress wasfurther confirmed in soil-based drought assays, in which the plantsoverexpressing G303 were found to be more tolerant to drought than thewild-type controls in the experiment (Table 12).

Utilities.

G303 may be useful for enhancing drought tolerance and seed germinationunder high salt conditions or other conditions of osmotic stress (forexample, freezing).

The G682 Subclade of Transcription Factor Polypeptides G682 (SEQ ID NO:233 and 234)

G682 was identified from the Arabidopsis BAC, AF007269, based onsequence similarity to other members of the Myb family within theconserved domain. G682 and closely-related clade member sequences eachcomprise a conserved Myb-related DNA-binding domain that is expected tofunction in a similar manner in each of these related sequences, thatis, by playing a central role in transcriptional regulation and in theconferring of shared traits.

Experimental Observations.

The function of G682 was analyzed through its ectopic overexpression inplants.

RT-PCR analysis of the endogenous levels of G682 transcripts indicatedthat this gene is expressed in all tissues tested, however, a very lowlevel of transcript is detected in roots and shoots. Array tissue printdata suggests that G682 is expressed primarily, but not exclusively, inflower tissue.

G682 overexpressors were glabrous and had tufts of more root hairs.

An array experiment was performed on G682 overexpressing line 5. Thedata from this one experiment indicates that this gene could be anegative regulator of chloroplast development and/or light dependentdevelopment because the gene Albino3 and many chloroplast genes arerepressed. Albino3 functions to regulate chloroplast development (PlantCell (1997) 9: 717-730). The gene G682 is itself is induced 20-fold.Other than a few additional transcription factors, very few genes areinduced as a result of the ectopic expression of G682. These plants arenot pale in color, making it uncertain how to relate the morphologicaland physiological data with the gene profiling data. The arrayexperiment needs to be repeated with additional lines.

The effects of a high salt environment (MS medium supplemented with 150mM NaCl) on the germination of G682 overexpressors and control seedlingswas studied. The results demonstrated that the overexpressors were moretolerant to the high salt concentration, being much larger and greenerthan controls. High sodium chloride growth assays often are used toindicate abiotic stress tolerance such as osmotic stress tolerance,including drought tolerance, which was subsequently confirmed withsoil-based drought assays conducted with plants overexpressing G682.

G682-overexpressing line were found to be larger and greener thanwild-type controls that were similarly treated in a cold germinationassay (8° C.), indicating enhanced tolerance of the former togermination in these cold conditions.

G682 overexpressors were larger and greener in sucrose germinationassays than wild-type controls, indicating that G682 overexpression canconfer a sugar-sensing or abiotic stress phenotype. This assay is usedto determine whether a plant has an altered sugar sensing response oraltered abiotic stress tolerance, and, in this case, indicates thatoverexpression of G682 can confer this phenotype in plants.

In a heat germination assay (32° C. to 37° C. for 6 hours of exposure),G682 overexpressing seedlings were significantly larger, greener and hadgreater cotyledon expansion than wild type seedlings. In subsequentexperiments, it was found that older plants were also more tolerant toheat stress compared to wild-type controls. At the time theseexperiments were performed, it was suggested that further experimentswere needed to address whether or not the heat germination phenotype ofthe G682 overexpressors was related to water deficit stress tolerance inthe germinating seedling, and correlated with a possible droughttolerance phenotype. More recent experiments have shown that G682overexpressors were, on average, more tolerant to water deprivationconditions in soil-based drought assays than wild-type plants (Table12), and two of three lines were significantly more drought tolerantthan the wild-type controls.

Utilities.

The utility of this gene and its equivalogs would be to confer salt,heat and cold tolerance to germinating seeds and plants, and droughttolerance in plants.

G1816 (SEQ ID NO: 311 and 312)

G1816 is a paralog of G682 from Arabidopsis. G1816 is a member of theMYB-related class of transcription factors. The gene corresponds toTRIPTYCHON (TRY), and has recently been shown to be involved in thelateral inhibition during epidermal cell specification in the leaf androot (Schellmann et al. (2002) EMBO J. 21: 5036-5046). The modelproposes that TRY (G1816) and CPC (G225) function as repressors oftrichome and atrichoblast cell fate. TRY loss-of-function mutants formectopic trichomes on the leaf surface. TRY gain-of-function mutants areglabrous and form ectopic root hairs. G1816 and closely-related Glademember sequences each comprise a conserved Myb-related DNA-bindingdomain that is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

The complete sequence of G1816 was determined. The function of the genewas studied using transgenic plants in which G1816 was expressed underthe control of the 35S promoter. Consistent with the morphologicalphenotypes published for the 35S::TRY overexpressors, the transgenicplants were glabrous and form ectopic root hairs.

The 35S::G1816 plants were also insensitive to growth retardationeffects of germination on conditions of high glucose and sucrose (MSmedium supplemented with 5% glucose and 9.4% sucrose, respectively); theoverexpressor seedlings were large and green, as contrasted with thewild-type control seedlings which were significantly smaller and morepigmented. This indicates that G1816 plays a role in sugar sensingresponses in the plant or osmotic stress tolerance.

A number of G1816 overexpressing lines were more tolerant to droughtconditions than wild-type controls in soil-based assays.

Utilities.

The phenotypic effects of G1816 overexpression, such as the increase inroot hair formation and the increase in seedling vigor observed in agermination assay on high glucose media, indicated that the gene or itsorthologs can be used to engineer plants with increased tolerance toabiotic stresses such as drought, salt, heat or cold.

In addition, the enhanced performance of G1816 overexpression linesunder low nitrogen conditions indicated that the gene or its orthologscould be used to engineer crops that could thrive under conditions ofreduced nitrogen availability. These assays also indicate that G1816 andits equivalogs are potential regulators of a plant's C/N sensing,nitrogen uptake and utilization, and its response to low nutrientconditions. For further analysis, see the discussion above: “PotentialApplications of Polynucleotides and Polypeptides that Regulate C/Nsensing”.

The effect of G1816 overexpression on insensitivity to glucose in agermination assay, indicated that the gene or its orthologs could beinvolved in sugar sensing responses in the plant.

G1816 or its orthologs could also be used to alter anthocyaninproduction and trichome formation in leaves.

The potential utilities of genes involved in anthocyanin productioninclude alterations in pigment production for horticultural purposes andincrease stress resistance perhaps in combination with othertranscription factors. Flavonoids have antimicrobial activity and couldbe used to engineer pathogen resistance. In addition, several flavonoidcompounds have health promoting effects such as the inhibition of tumorgrowth and cancer, prevention of bone loss and the prevention of theoxidation of lipids.

G3450 (SEQ ID NO: 319 and 320)

G3450 is a soy ortholog or G682. Almost all of the 35S::G3450 linesexamined were glabrous and had more root hair than controls, thusexhibiting a morphology similar to G682. G3450 and closely-related clademember sequences each comprise a conserved Myb-related DNA-bindingdomain that is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

In plate-based assays, G3450 overexpressors were more tolerant togermination and growth in cold conditions, and growth in heat.

At least four lines of G3450 overexpressors were more tolerant todrought treatment than wild-type controls in soil-based assays. Afterrewatering, these same lines also exhibited much superior recovery fromthe effects of the drought treatment than the controls, as evidenced bytheir return to vigor (many of the control plants were dead at thispoint).

Utilities.

Similar to other members of the G682 subclade, G3450 or its equivalogscan be used to engineer plants with increased tolerance to abioticstresses such as drought, heat or cold.

Summary of Drought Assay Results

Table 11 presents the results obtained in an assay in which Arabidopsisplants were subjected to water deprivation for seven to eight days. Atthe end of this dry-down period, each pot was assigned a numeric scoredepending on the health of its plants. A score of 0 to 6 was assignedbased on a plant's color and general appearance, with plants that wereall brown receiving a “0” and, at the other end of the spectrum, plantsthat had an excellent appearance (all green) receiving a “6”. The meanof the recorded numeric score of all pots of a given genotype per lineof all flats tested is presented in order of decreasing health.

TABLE 11 Comparison of recorded numeric score plants subjected todrought treatment. GID Mean score G2133 5.875 G634 4.778 G922 4.667 G9164.6 G1274 4.273 G864 3.733 G2999 3.7 G2992 3.7 G353 3.6 G47 3.459 G20533.404 G975 3.393 G489 3.364 G1792 3.281 G1820 3.2 G2453 3.2 G2140 3.139G2701 3.108 G3086 3.056 G611 3.048 G1452 3.042 G481 3.041 G624 3.000G2854 2.829 G303 2.812 G2839 2.783 G2789 2.708 G188 2.692 G325 2.556G2776 2.513 G175 2.467 G2110 2.432 G1206 2.412 G682 2.381 G1730 2.341G2969 2.333 G2998 2.333 G1069 2.316 Wild-type 2.284

Table 12 compares the survival ratings of Arabidopsis plantsoverexpressing various polypeptides, evaluated after seven to eight daysof drought treatment, rewatering, and two to three days of a recoveryperiod Values indicate the median odds of survival within a given flat(the 50th percentile of survival within each pot of a given genotype perline divided by the average wild-type survival in the flat).

TABLE 12 Survival ratings of Arabidopsis plants after drought andrewatering treatment GID Median per flat G2133 3.365 G1274 2.059 G9221.406 G2999 1.255 G3086 1.179 G354 1.167 G1792 1.161 G2053 1.091 G9751.090 G1069 1.037 G916 1.023 G2701 1.000 G1820 1.000 G47 0.921 G28540.889 G2789 0.845 G481 0.843 G634 0.834 G175 0.814 G2839 0.805 G14520.803 Wild-type 0.800

Example IX: Results of C/N Sensing Assays

This example provides experimental evidence for altered carbon-nitrogenbalance controlled by transcription factor polypeptides and polypeptidesof the invention.

The G682 Subclade of Transcription Factor Polypeptides G682 (SEQ ID NO:233 and 234)

G682 was identified from the Arabidopsis BAC, AF007269, based onsequence similarity to other members of the Myb family within theconserved domain. G682 and closely-related clade member sequences eachcomprise a conserved Myb-related DNA-binding domain that is expected tofunction in a similar manner in each of these related sequences, thatis, by playing a central role in transcriptional regulation and in theconferring of shared traits.

Experimental Observations.

The function of G682 was analyzed through its ectopic overexpression inplants.

RT-PCR analysis of the endogenous levels of G682 transcripts indicatedthat the gene is expressed in all tissues. However, only a very lowlevel of transcript was detected in roots and shoots. The function ofG682 was analyzed through its ectopic overexpression. 35S::G682 lineswere glabrous, had tufts of increased root hair density and showedbetter germination under drought related stress (heat). In one of thegenomics experiments, it was also noted that 35S::G682 lines showed aslightly enhanced performance on potassium limited media.

We have now analyzed 35S::G682 seedlings in a C/N sensing assay bycomparing the effects of G682-overexpressing lines germinating on N−/Smedium (MS media minus nitrogen plus 3% sucrose) with control wild-typeseedlings on the same medium. The overexpressors of these lines werefound to produce much less anthocyanin, indicating that G682 likely hasa role in nitrogen utilization and in the response to low nutrientconditions.

The phenotypic effects described for 35S::G682 overexpressing plants inthe C/N sensing assay is similar to that observed for 35S lines fromother members of the G682 subclade (G226, G682, G1816, and 2718).Similarly, plants that overexpress any of the G682 Arabidopsis 35S CaMVclade members have been observed to have increased root hair formationand reduced anthocyanin levels in C/N sensing assays. Additionally,Arabidopsis G682 subclade member (Table 13) and non-Arabidopsis G682subclade members, including soy and corn sequences, have also been shownin laboratory experiments to confer tolerance to various abioticstresses (Table 13).

Thus, the entire clade of G682-related genes appear to have very relatedfunctions and those that have been so tested have been shown to beinvolved in the response to nitrogen limitation. As such, thesesequences are likely to be good candidates for improving the efficiencyof nutrient utilization and tolerance to other stresses in commercialcrops. Thus, the G682-related genes could afford yield savings viamultiple different traits.

Table 13 lists the results obtained in several abiotic stress assays inwhich a number of members of the G682 subclade were overexpressed inArabidopsis plants. For all genes, assays were performed in whichexpression was under the control of the cauliflower mosaic virus 35Stranscription initiation region. For G682, assays were also performedwith transgenic plants in which expression was controlled as indicatedin the second column. Control of expression of G682 was performed usingARSK1, a root-specific protein kinase gene promoter, the CUT1 promoter,which controls production of epicuticular wax in bolting stems and isused for epidermis-specific expression, and by superactivation, in whichan expression vector having a GAL4 activation domain is fused to theG682 sequence to create an N-terminal GAL4 activation domain proteinfusion. The first and second columns identify the sequence test by SEQID NO: and Gene Identification Number. The third column identifies thespecies in which the gene originated. The fourth through eleventhcolumns list the ratio of transgenic Arabidopsis lines with an alteredphenotype relative to controls, over the number of lines tested. Theseresults show increased germination in high salt, increased germinationin high mannitol, increased germination in high sucrose, decreasedsensitivity to ABA, increased germination in heat, increased toleranceto heat in a growth assay, increased germination in cold conditions, andincreased tolerance to cold in a growth assay (chilling), respectively.The column labeled “C/N” identifies the sequences that were tested andconferred altered C/N sensing of the plants (in each of these case, lessanthocyanin was produced by the seedlings in the C/N sensing assays).“Low N tol.” refers to decreased sensitivity, relative to controls, tolow nitrogen conditions in plate-based assays. The column labeled“Morph” identifies the sequences that exhibited a glabrous phenotypewith increased root hairs, the latter being of particular interest inthat this trait may help confer abiotic stress tolerance. The lastcolumn indicates the lines that were positive in a soil-based droughtassay.

TABLE 13 Results of abiotic stress experiments with G682-relatedsequences Germ Germ Grth Germ Grth SEQ ID in in in in in C/N Low NDrought NO: GID Species NaCl Mann Sucr ABA Heat Heat Cold cold sens tol.Morph tol. 234 35S::G682 A. thaliana 9/10 3/10 10/10  6/10 3/10 0/100/10 0/10 + nc + + 234 ARSK1::G682 A. thaliana 0/10 0/10 0/10 0/10 0/100/10 2/10 0/10 nc nc wt + 234 CUT1::G682 A. thaliana 6/10 0/10 0/10 0/100/10 0/10 1/10 0/10 nc nc wt wt 234 SA G682 A. thaliana 2/10 0/10 0/100/10 0/10 1/10 0/10 0/10 nc nc + wt 285 G226 A. thaliana 0/9  0/9  5/9 8/9  0/9  0/9  2/9  2/9  + + + nc 286 G1816 A. thaliana 0/10 0/10 10/10 0/10 0/10 0/10 0/10 0/10 + + + nc 323 G2718 A. thaliana nc nc nc nc ncnc nc nc + + + nc 324 G3393 Oryza sativa 0/10 0/10 1/10 0/10 0/10 0/100/10 0/10 nc nc + nc 360 G3431 Z. mays 0/10 0/10 4/10 0/10 2/10 0/100/10 0/10 nc nc + nc 360 G3444 Z. mays 0/10 0/10 0/10 0/10 2/10 2/100/10 1/10 nc nc + nc 378 G3448 G. max 0/10 0/10 0/10 0/10 0/10 0/10 0/103/10 nc nc + + 380 G3449 G. max 1/10 0/10 0/10 0/10 1/10 0/10 3/10 1/10nc nc + nc 382 G3450 G. max 2/10 0/10 0/10 0/10 1/10 3/10 6/10 5/10 ncnc + + Symbols and abbreviations: + phenotype observed wt result notsignificantly different from wild-type Grth Growth Germ germination Toltolerance Morph morphology C/N sens carbon/nitrogen balance sensing Manngrowth in high mannitol Sucr growth in high sucrose ABA reducedsensitivity to abscisic acid SA superactivation nc assay results notcompleted or performed to date

Utilities

The utility of this gene and its equivalogs would be to confer heattolerance to germinating seeds and drought tolerance in plants.

These assays also indicate that G682 and its equivalogs are potentialregulators of a plant's C/N sensing, nitrogen uptake and utilization,and its response to low nutrient conditions. For further analysis, seethe discussion above: “Potential Applications of Polynucleotides andPolypeptides that Regulate C/N sensing”.

G682 equivalogs include, for example, Arabidopsis thaliana SEQ ID NO:286, 312 and 324 (G226, G1816 and G2718); Oryza sativa (japonicacultivar-group) SEQ ID NO: 326 and 328 (G3392 and G3393); Glycine maxSEQ ID NO: 372, 374, 376, 378, 380, and 382 (G3445, G3446, G3447, G3448,G3449, and G3450); and Zea mays SEQ ID NO: 360 and 370 (G3431 andG3444).

G226 (SEQ ID NO: 285 and 286)

G226 is a paralog of G682 from Arabidopsis. G226 (AT2G30420) wasidentified from the Arabidopsis BAC sequence (GenBank accessionAC002338), based on sequence similarity within the conserved domain toother Myb family members in Arabidopsis. G226 and closely-related clademember sequences each comprise a conserved Myb-related DNA-bindingdomain that is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR expression analysis of the endogenous levels of G226 indicatedthat the gene is primarily expressed in leaf tissue. The function ofG226 was analyzed through its ectopic overexpression. G226overexpressors were more tolerant to conditions of high salt (Table 13)and low nitrogen (Table 14). The overexpressors were larger and greenerand had more root growth and root hairs under conditions of nitrogenlimitation than wild-type controls. Many plants were glabrous and lackedanthocyanin production when under stress such as growth conditions oflow nitrogen (the medium contained 20 mg/L of NH₄(NO₃) as the nitrogensource).

G226 also showed a salt tolerance phenotype in plate-based salt stressassays (MS medium supplemented with 150 mM NaCl). 35S::G226 seedlingsgenerally appeared larger and greener than wild-type seedlings, thelatter being generally smaller with less root mass, and were morechlorotic.

We have now analyzed 35S::G226 seedlings in a C/N sensing assay.Anthocyanin accumulation was significantly less than that observed incontrol wild-type seedlings, confirming that this gene has a role in theresponse to nutrient limited conditions. It should be noted that othermembers of the clade (G226, G682, G1816, G2718 and non-Arabidopsisorthologs) produce similar effects when overexpressed (Tables 13 and14).

Utilities.

These assays indicate that G226 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

In addition, this gene and its equivalogs could be used to alter seedprotein amounts and/or composition, which could impact yield as well asthe nutritional value and production of various food products.

G1816 (SEQ ID NO: 311 and 312)

G1816 is a paralog of G682 from Arabidopsis. G1816 is a member of theMYB-related class of transcription factors. The gene corresponds toTRIPTYCHON (TRY), and has recently been shown to be involved in thelateral inhibition during epidermal cell specification in the leaf androot (Schellmann et al. (2002) EMBO J. 21: 5036-5046). The modelproposes that TRY (G1816) and CPC (G225) function as repressors oftrichome and atrichoblast cell fate. TRY loss-of-function mutants formectopic trichomes on the leaf surface. TRY gain-of-function mutants areglabrous and form ectopic root hairs. G1816 and closely-related Glademember sequences each comprise a conserved Myb-related DNA-bindingdomain that is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

The complete sequence of G1816 was determined. The function of the genewas studied using transgenic plants in which G1816 was expressed underthe control of the 35S promoter. Consistent with the morphologicalphenotypes published for the 35S::TRY overexpressors, the transgenicplants were glabrous and form ectopic root hairs.

These transgenic lines were also more tolerant to growth undernitrogen-limiting conditions, both in a germination assay as well as aroot growth assay on older seedlings.

In addition to the nitrogen-limiting tolerance phenotypes observed inthese transgenic lines, the 35S::G1816 plants were also insensitive togrowth retardation effects of germination on conditions of high glucose(MS medium supplemented with 5% glucose); the overexpressor seedlingswere large and green, as contrasted with the wild-type control seedlingswhich were significantly smaller and more pigmented. This indicates thatG1816 plays a role in sugar sensing responses in the plant or osmoticstress tolerance. Genes for many sugar-sensing mutants are allelic togenes involved in abscisic acid and ethylene signaling (Rolland et al.(2002) Plant Cell 14: Suppl. S185-S205). Therefore, G1816 could also beinvolved in hormone signaling pathways.

We have now analyzed 35S::G1816 seedlings in a C/N sensing assay. Theseedlings in these experiments were germinated on N−/S/Gln medium (MSmedia minus nitrogen plus 3% sucrose and 1 mM glutamine). The G1816overexpressing seedlings were found to have less anthocyanin than thecontrol seedlings, indicating that G1816 likely has a role in nitrogenutilization and in the response to low nutrient conditions.

Germination assays were also used to compare G1816 overexpressors andwild-type control seedlings on a low nitrogen medium. The overexpressorswere much larger, had no anthocyanin and produced more root growth androot hair density than the wild-type controls.

Utilities.

The phenotypic effects of G1816 overexpression, such as the increase inroot hair formation and the increase in seedling vigor observed in agermination assay on high glucose media, indicated that the gene or itsorthologs can be used to engineer plants with increased tolerance toabiotic stresses such as drought, salt, heat or cold.

In addition, the enhanced performance of G1816 overexpression linesunder low nitrogen conditions indicated that the gene or its orthologscould be used to engineer crops that could thrive under conditions ofreduced nitrogen availability. These assays also indicate that G1816 andits equivalogs are potential regulators of a plant's C/N sensing,nitrogen uptake and utilization, and its response to low nutrientconditions. For further analysis, see the discussion above: “PotentialApplications of Polynucleotides and Polypeptides that Regulate C/Nsensing”.

The effect of G1816 overexpression on insensitivity to glucose in agermination assay, indicated that the gene or its orthologs could beinvolved in sugar sensing responses in the plant.

G1816 or its orthologs could also be used to alter anthocyaninproduction and trichome formation in leaves.

The potential utilities of genes involved in anthocyanin productioninclude alterations in pigment production for horticultural purposes andincrease stress resistance perhaps in combination with othertranscription factors. Flavonoids have antimicrobial activity and couldbe used to engineer pathogen resistance. In addition, several flavonoidcompounds have health promoting effects such as the inhibition of tumorgrowth and cancer, prevention of bone loss and the prevention of theoxidation of lipids.

G2718 (SEQ ID NO: 323 and 324)

G2718 is a paralog of G682 from Arabidopsis. G2718 (AT1G01380) wasidentified in the BAC clone, F6F3 (GenBank accession AC023628). Twohighly related genes, TRY and CPC have been implicated in epidermal cellspecification. A lateral inhibition model proposes that TRY (G1816) andCPC (G225) function as repressors of trichome and atrichoblast cell fate(Shellmann et al. (2002) EMBO J. 21: 5036-5046). A comprehensive reviewon epidermal cell-fate specification has been published recently(Schiefelbein (2003) Curr. Opin. Plant Biol. 6: 74-78). G2718 andclosely-related clade member sequences each comprise a conservedMyb-related DNA-binding domain that is expected to function in a similarmanner in each of these related sequences, that is, by playing a centralrole in transcriptional regulation and in the conferring of sharedtraits.

Experimental Observations.

Results obtained by the overexpression of G1816 in plants, includingabiotic stress tolerance and low nitrogen tolerance phenotypes have beenpreviously reported in U.S. patent application Ser. No. 10/714,887,filed Nov. 13, 2003.

The function of G2718 was studied using plants in which the gene wasexpressed under the control of the 35S promoter. Overexpression of G2718resulted in a glabrous phenotype. The effect was highly penetrant, beingobserved in all primary transformants and each of three independent T2lines. All of the T1 lines showed a very strong phenotype and completelylacked trichomes on leaves and stems. A comparably severe effect wasobserved in one of the three T2 populations, whereas the other two T2populations each exhibited a weaker phenotype, indicating that theeffect might have become partially silenced between the generations.Trichomes were present in these weaker lines, but at a much lowerdensity than in wild type.

In addition to the effects on trichome density, 35S::G2718 transformantswere also generally slightly smaller than wild type controls.

The phenotypic effects above were observed in the 35S::G2718 as well asin all 35S lines from members of the G2718 clade (G225, G226, G1816, andG682). Similarly, 35S::TF lines from the G2718 clade all had increasedroot hair formation, reduced anthocyanin levels, and showed improvedgrowth under nitrogen limiting conditions.

Overexpressors were generally larger, had more root mass, and were oftengreener than wild-type control seedlings on low nitrogen media,indicating that overexpression of G2718 confers enhanced tolerance ofplants to this low nutrient condition, possibly by improving nutrientuptake.

We have now analyzed 35S::G2718 seedlings in a C/N sensing assay.Anthocyanin accumulation was significantly less than that observed incontrol plants (Table 14), indicating that G2718 likely has a role innitrogen utilization and in the response to low nutrient conditions.

Utilities.

The phenotypic effects of G2718 overexpression, such as the increase inroot hair formation and the increase in seedling vigor observed in aroot growth assay on N-limiting media, indicates that the gene or itsequivalogs could be used to engineer plants with increased tolerance toabiotic stresses such as nutrient limitation, drought, salt, heat orcold.

The enhanced performance of G2718 overexpression lines under lownitrogen conditions indicates that the gene or its equivalogs could beused to engineer crops that could thrive under conditions of reducednitrogen availability. These assays also indicate that G2718 and itsequivalogs are potential regulators of a plant's C/N sensing, nitrogenuptake and utilization, and its response to low nutrient conditions. Forfurther analysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

G2718 or its equivalogs could also be used to alter anthocyaninproduction or trichome formation. and production of secondarybiochemicals (e.g., lipophilic terpenes) by trichomes.

G3392 (SEQ ID NO: 325 and 326)

G3392 is a rice ortholog of G682. G3392 and closely-related clade membersequences each comprise a conserved Myb-related DNA-binding domain thatis expected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

Similar to G682 and other homologs of G3392, a number ofG3392-overexpressing lines displayed reduced leaf trichomes and moreroot hairs.

On low nitrogen media, Arabidopsis seedlings overexpressing G3392accumulated less anthocyanin than wild-type control seedlings. G3392overexpressors also accumulated less anthocyanin on low nitrogen MSmedia minus nitrogen and supplemented with either 3% sucrose, or 3%sucrose and 1 mM glutamine, indicating an altered C/N sensing phenotype.

In heat germination assays and in assays conducted with more matureplants conducted at 32° C., G3392-overexpressing Arabidopsis seedlingswere greener than wild-type controls. The results of this assay indicatethat, similar to other members of the clade, the monocot-derived G3392has the ability to confer tolerance to heat stress in plants.

G3392-overexpressing Arabidopsis plants were also more tolerant to 300mM mannitol and 9.4% sucrose than wild-type control plants grown inplate based-assays under similar conditions, indicating a sugar-sensingand osmotic stress tolerant phenotype.

In heat germination assays and in assays conducted with more matureplants conducted in media containing 150 mM NaCl, G3392-overexpressingArabidopsis seedlings were larger greener than wild-type controls.

In cold germination assays for 6 hours at 8° C. and in assays conductedwith more mature plants conducted with a 6 hour exposure to 4-8° C.,G3392-overexpressing Arabidopsis seedlings accumulated much lessanthocyanin than wild-type controls. The results of this assay indicatethat, similar to other members of the Glade, the monocot-derived G3392has the ability to confer tolerance to cold stress in plants.

Utilities.

The phenotypic effects of G3392 overexpression indicates that the geneor its equivalogs could be used to engineer plants with increasedtolerance to several abiotic stresses and low nitrogen conditions.

G3393 (SEQ ID NO: 327 and 328)

G3393 is a rice ortholog of G682. G3393 and closely-related clade membersequences each comprise a conserved Myb-related DNA-binding domain thatis expected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

Similar to G682 and other homologs of G3393, a number ofG3393-overexpressing lines displayed reduced leaf trichomes and moreroot hairs.

On low nitrogen media, Arabidopsis seedlings overexpressing G3393accumulated significantly less anthocyanin than wild-type controlseedlings. G3393 overexpressors also accumulated less anthocyanin on lownitrogen MS media minus nitrogen and supplemented with either 3%sucrose, or 3% sucrose and 1 mM glutamine, indicating an altered C/Nsensing phenotype.

In cold germination assays for 6 hours at 8° C. and in assays conductedwith more mature plants conducted with a 6 hour exposure to 4-8° C.,G3393-overexpressing Arabidopsis seedlings accumulated much lessanthocyanin than wild-type controls. The results of this assay indicatethat, similar to other members of the Glade, the monocot-derived G3393has the ability to confer tolerance to cold stress in plants.

Utilities.

The phenotypic effects of G3393 overexpression indicates that the geneor its equivalogs could be used to engineer plants with increasedtolerance to cold stress and low nitrogen conditions.

G3431 (SEQ ID NO: 359 and 360)

G3431 is a corn ortholog of G682. G3431 and closely-related clade membersequences each comprise a conserved Myb-related DNA-binding domain thatis expected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

Similar to G682 and other homologs of G3431, a number ofG3431-overexpressing lines displayed reduced leaf trichomes and moreroot hairs.

On low nitrogen media, Arabidopsis seedlings overexpressing G3431accumulated significantly less anthocyanin than wild-type controlseedlings. G3431 overexpressors also accumulated less anthocyanin on lownitrogen MS media minus nitrogen and supplemented with either 3%sucrose, or 3% sucrose and 1 mM glutamine, indicating an altered C/Nsensing phenotype.

In cold germination assays for 6 hours at 8° C. and in assays conductedwith more mature plants conducted with a 6 hour exposure to 4-8° C.,G3431-overexpressing Arabidopsis seedlings accumulated much lessanthocyanin than wild-type controls. The results of this assay indicatethat, similar to other members of the Glade, the monocot-derived G3431has the ability to confer tolerance to cold stress in plants.

In osmotic stress assays conducted on MS media containing 9.4% sucrose,G3431-overexpressing Arabidopsis seedlings were greener and accumulatedless anthocyanin than wild-type controls, indicating osmotic stresstolerance was conferred by overexpressing G3431.

Utilities.

The phenotypic effects of G3431 overexpression indicates that the geneor its equivalogs could be used to engineer plants with increasedtolerance to cold and osmotic stress and low nitrogen conditions.

G3444 (SEQ ID NO: 369 and 370)

G3444 is a corn ortholog of G682. G3444 and closely-related clade membersequences each comprise a conserved Myb-related DNA-binding domain thatis expected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

Similar to G682 and other homologs of G3444, a number ofG3444-overexpressing lines had reduced trichomes.

On low nitrogen media, Arabidopsis seedlings overexpressing G3444accumulated less anthocyanin than wild-type control seedlings. One lineof G3444 overexpressors also accumulated less anthocyanin on lownitrogen MS media minus nitrogen and supplemented with either 3%sucrose, or 3% sucrose and 1 mM glutamine, indicating an altered C/Nsensing phenotype.

In heat germination assays and in assays conducted with more matureplants conducted at 32° C., G3444-overexpressing Arabidopsis seedlingswere greener than wild-type controls. The results of this assay indicatethat, similar to other members of the clade, the monocot-derived G3444has the ability to confer tolerance to abiotic stress in plants.

Utilities.

The phenotypic effects of G3444 overexpression indicates that the geneor its equivalogs could be used to engineer plants with increasedtolerance to heat and low nitrogen conditions.

G3445 (SEQ ID NO: 371 and 372)

G3445 is a soy ortholog of G682. G3445 and closely-related clade membersequences each comprise a conserved Myb-related DNA-binding domain thatis expected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

Similar to G682 and other homologs of G3445, a number ofG3445-overexpressing lines had reduced trichomes.

In germination assays conducted on media supplemented with 0.3 μM ABA,G3445-overexpressing Arabidopsis seedlings were larger and greener thanwild-type controls.

Utilities.

The phenotypic effects of G3445 overexpression indicates that the geneor its equivalogs could be used to engineer plants with increasedtolerance to osmotic stress conditions.

G3448 (SEQ ID NO: 377 and 378)

G3448 is a soy ortholog of G682. G3448 and closely-related clade membersequences each comprise a conserved Myb-related DNA-binding domain thatis expected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

Similar to G682 and other homologs of G3448, a number ofG3448-overexpressing lines displayed reduced leaf trichomes and moreroot hairs.

On low nitrogen media, Arabidopsis seedlings overexpressing G3448accumulated significantly less anthocyanin than wild-type controlseedlings. G3448 overexpressors also accumulated less anthocyanin on lownitrogen MS media minus nitrogen and supplemented with either 3%sucrose, or 3% sucrose and 1 mM glutamine, indicating an altered C/Nsensing phenotype.

In assays conducted with Arabidopsis plants at a 6 hour exposure to 4-8°C., G3448-overexpressing Arabidopsis seedlings accumulated lessanthocyanin than wild-type controls. The results of this assay indicatethat, similar to other members of the clade, the dicot-derived G3448 hasthe ability to confer tolerance to cold stress in plants.

Utilities.

The phenotypic effects of G3448 overexpression indicates that the geneor its equivalogs could be used to engineer plants with increasedtolerance to cold stress and low nitrogen conditions.

G3449 (SEQ ID NO: 379 and 380)

G3449 is a soy ortholog of G682. G3449 and closely-related clade membersequences each comprise a conserved Myb-related DNA-binding domain thatis expected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

Similar to G682 and other homologs of G3393, a number ofG3393-overexpressing lines displayed reduced leaf trichomes and moreroot hairs.

On low nitrogen media, Arabidopsis seedlings overexpressing G3449accumulated significantly less anthocyanin than wild-type controlseedlings. G3449 overexpressors also accumulated less anthocyanin on lownitrogen MS media minus nitrogen and supplemented with either 3%sucrose, or 3% sucrose and 1 mM glutamine, indicating an altered C/Nsensing phenotype.

In cold germination assays for 6 hours at 8° C., G3449-overexpressingArabidopsis seedlings accumulated much less anthocyanin than wild-typecontrols. The results of this assay indicate that, similar to othermembers of the clade, the dicot-derived G3449 has the ability to confertolerance to cold stress in plants.

Utilities.

The phenotypic effects of G3449 overexpression indicates that thissequence or its equivalogs could be used to engineer plants withincreased tolerance to cold stress and low nitrogen conditions.

G3450 (SEQ ID NO: 381 and 382)

G3450 is a soy ortholog of G682. G3450 and closely-related clade membersequences each comprise a conserved Myb-related DNA-binding domain thatis expected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations

Similar to G682 and other homologs of G3450, a number ofG3450-overexpressing lines displayed reduced leaf trichomes and moreroot hairs.

On low nitrogen media, Arabidopsis seedlings overexpressing G3392accumulated less anthocyanin than wild-type control seedlings. G3450overexpressors also accumulated less anthocyanin on low nitrogen MSmedia minus nitrogen and supplemented with either 3% sucrose, or 3%sucrose and 1 mM glutamine, indicating an altered C/N sensing phenotype.

In cold germination assays for 6 hours at 8° C. and in assays conductedwith more mature plants conducted with a 6 hour exposure to 4-8° C.,G3450-overexpressing Arabidopsis seedlings accumulated much lessanthocyanin than wild-type controls. The results of this assay indicatethat, similar to other members of the clade, the dicot-derived G3450 hasthe ability to confer tolerance to cold stress in plants.

In heat germination assays and in assays conducted with more matureplants conducted at 32° C., G3450-overexpressing Arabidopsis seedlingswere greener than wild-type controls. The results of this assay indicatethat, similar to other members of the clade, the dicot-derived G3450 hasthe ability to confer tolerance to heat stress in plants.

G3450-overexpressing Arabidopsis plants were also more tolerant to saltand desiccation than wild-type control plants grown under similarconditions in plate based-assays, and to drought conditions insoil-based assays.

Utilities.

The phenotypic effects of G3450 overexpression indicates that thissequence or its equivalogs could be used to engineer plants withincreased tolerance to low nitrogen conditions, salt, cold stress, heatstress, and low water conditions.

The G24 Clade of Transcription Factor Polypeptides G24 (SEQ ID NO: 419and 420)

G24 corresponds to gene At2g23340 (AAB87098). G24 and closely-relatedclade member sequences each comprise a conserved AP2 DNA-binding domainthat is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

Based on RT-PCR expression analysis, G24 was found to be ubiquitouslyexpressed at low levels in germinating seedlings. The function of G24was studied using transgenic plants in which the gene was expressedunder the control of the 35S promoter. 35S::G24 seedlings oftendeveloped black necrotic tissue patches on cotyledons and leaves, andmany died at that stage. Some 35S::G24 seedlings exhibited a weakerphenotype, and although necrotic patches were visible on the cotyledons,they did not die. These seedlings developed into plants that wereusually small, slow growing, and poorly fertile in comparison to wildtype controls. The leaves of older 35S::G24 plants were also observed tobecome yellow and senesce prematurely compared to wild type. Of thelines sent for physiological assays, all showed a comparable response towild-type. However, 35S::G24 line 2 seedlings became necrotic and diedimmediately after germination on MS plates. 35S::G24 line 8 has anintermediate phenotype in which the seedlings develop some necroticlesions but survived and 35S::G24 line 11 seedlings appeared wild-type.

We have now analyzed 35S::G24 seedlings in a C/N sensing assay.Anthocyanin accumulation was slightly less than that observed in controlwild-type seedlings (Table 14), indicating that the gene may be involvedin the response to low nutrient conditions.

Utilities.

These assays indicate that G24 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G154 Clade of Transcription Factor Polypeptides G154 (SEQ ID NO: 421and 422)

G154 was identified in the sequence of BAC F17K2, from chromosome 2(gene At2g45660). It also corresponds to SUPPRESSOR OF OVEREXPRESSION OFCO (SOC1), and was previously designated AGL20 (Samach et al. (2000)Science. 288: 1613-1616; Lee et al. (2000) Genes Dev. 14:2366-2376;Borner et al. (2000) Plant J. 24: 591-599). This gene has been isolatedseveral times in genetic and molecular screens for flowering-timemutants. SOC1/AGL20 was identified by suppression subtractionhybridization as a direct target of the zinc finger transcription factorCONSTANS (Samach et al. (2000) supra), and also genetically as a lateflowering mutant capable of suppressing the phenotype caused byoverexpression of CO (hence the name SOC1) (Onouchi et al. (2000) PlantCell 12: 885-900). The gene was also identified as a dominant FRIGIDA(FRI) suppressor in activation tagging mutagenesis (Lee et al. (2000)supra), as well as a late flowering mutant generated by transposontagging (Borner et al. (2000) supra). Genetic and molecular analyseshave allowed the position of this gene within the flowering-time controlnetwork to be determined.

Samach et al. (Samach et al. (2000) supra) reported that flowering istriggered by endogenous and environmental signals. CO promotes floweringof Arabidopsis in response to day length. Early target genes of co wereidentified using a steroid-inducible version of the protein. Two ofthese genes, SOC1 and FLOWERING LOCUS T (FT), are required for CO topromote flowering. SOC1 and FT are also regulated by a secondflowering-time pathway that acts independently of CO. Thus, early targetgenes of CO define common components of distinct flowering-timepathways.

Lee et al. (Lee (2000) supra) reported that the very late-floweringbehavior of Arabidopsis winter-annual ecotypes is conferred mainly bytwo genes, FRI and FLOWERING LOCUS C (FLC). AGL20 was identified as adominant FRI suppressor in activation tagging mutagenesis.Overexpression of AGL20 suppresses not only the late flowering of plantsthat have functional FRI and FLC alleles but also the delayed phasetransitions during the vegetative stages of plant development.Interestingly, AGL20 expression is positively regulated not only by theredundant vernalization and autonomous pathways of flowering but also bythe photoperiod pathway. Our results indicate that AGL20 is an importantintegrator of three pathways controlling flowering in Arabidopsis.

Borner et al. (Borner et al. (2000) supra) reported that the floweringtime in many plants is triggered by environmental factors that lead touniform flowering in plant populations, ensuring higher reproductivesuccess. So far, several genes have been identified that are involved inflowering time control. AGL20 is activated in shoot apical meristemsduring the transition to flowering. By transposon tagging we haveidentified late flowering agl20 mutants, showing that AGL20 is involvedin flowering time control. In previously described late floweringmutants of the long-day and constitutive pathways of floral inductionthe expression of AGL20 is down-regulated, demonstrating that AGL20 actsdownstream to the mutated genes. Moreover, we can show that AGL20 isalso regulated by the gibberellin (GA) pathway, indicating that AGL20integrates signals of different pathways of floral induction and mightbe a central component for the induction of flowering. In addition, theconstitutive expression of AGL20 in Arabidopsis is sufficient forphotoperiod independent flowering and the over-expression of theorthologous gene from mustard, MADSA, in the classical short-day tobaccoMaryland Mammoth bypasses the strict photoperiodic control of flowering.

G154 and closely-related clade member sequences each comprise aconserved MADS DNA-binding domain that is expected to function in asimilar manner in each of these related sequences, that is, by playing acentral role in transcriptional regulation and in the conferring ofshared traits.

Experimental Observations.

The function of G154 was studied using transgenic plants in which thegene was expressed under the control of the 35S promoter. Overexpressionof G154 produced a range of morphological effects. Early flowering wasnoted in a small number of primary transformants. Additionally,35S::G154 lines were sometimes small, spindly and poorly fertile. G154overexpressing lines behave similarly to wild-type controls in allphysiological and biochemical assays performed.

SOC1 has a well-established role in regulation of the onset offlowering. We have now analyzed 35S::G154 seedlings in a C/N sensingassay. Anthocyanin accumulation was slightly less than that observed incontrol wild-type seedlings in all three lines tested (Table 14). Thus,in addition to its effects on flowering time, this gene might alsoinfluence the response to low nutrient conditions.

Utilities.

These assays indicate that G154 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G384 Clade of Transcription Factor Polypeptides G384 (SEQ ID NO: 423and 424)

G384, also called ATML1 (Lu et al. (1996) Plant Cell 8:2155-2168),belongs to the HD-GL2 class of homeodomain proteins. It was isolatedbased on its homology to 039, a homeodomain protein from orchid.Northern blot analysis indicated that it was floral bud specific inArabidopsis and in situ hybridization data showed that G384 was onlyexpressed in the L1 layer of the shoot meristems and the protoderms ofthe pre-torpedo stage embryos. G384 and closely-related clade membersequences each comprise a conserved homebox DNA binding domain (or“homeodomain”) and a START domain that are expected to function in asimilar manner in each of these related sequences, that is, by playing acentral role in transcriptional regulation and in the conferring ofshared traits.

Experimental Observations.

35S::G384 lines showed developmental abnormalities including fusedorgans. We have now analyzed the function of G384 by characterizingoverexpression lines in C/N sensing assays. These lines showed increasedsensitivity and elevated anthocyanin levels relative to wild-type (Table14). It is possible, however, that G384 is not specifically involved ina C/N sensing response since addition of glutamine to the growth platesdid not alleviate the phenotype. It should be emphasized that G384 is amember of the HD-GL2 class of homeodomain proteins. Overexpression linesfor two other HD-GL2 class genes, G1535 and G707, showed comparablephenotypes to the 35S::G384 lines studied in the present screen. Thesefindings are of particular interest because GL2 acts in the geneticpathway through which the CAPRICE (CPC) related genes regulate rootdevelopment. The current results indicate that as well as GL2 itself,other homeodomain proteins from the HD-GL2 class might also act inpathways involving the CAPRICE (CPC) related genes, given that theCAPRICE (CPC) related genes influence nutrient limitation responses andanthocyanin production.

Utilities.

These assays indicate that G384 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G486 Clade of Transcription Factor Polypeptides G486 (SEQ ID NO: 293and 294)

G486 was identified as a BAC sequence (AC000106) with homology toCCAAT-like transcription factors. G486 and closely-related clade membersequences each comprise a conserved CBFD_NFYB_HMF domain that isexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR expression analysis indicated that G486 is expressed primarily inroots, flowers, cauline leaves and seedlings. The function of G486 wasanalyzed through by the generation of 35S::G486 overexpressing plants.35S::G486 lines were noted to be somewhat small, rather darker green,and were delayed in the onset of flowering.

We have now analyzed 35S::G486 seedlings in a C/N sensing assay.Anthocyanin accumulation was less than that observed in controlwild-type seedlings in one line of two lines tested, indicating thatoverexpression of G486 in Arabidopsis gave a mild response in overcomingthe stress caused by this assay (Table 14).

Utilities.

These assays indicate that G486 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G545 Clade of Transcription Factor Polypeptides G545 (SEQ ID NO: 425and 426)

G545 was discovered independently by two groups. Lippuner et al.(Lippuner et al. (1996) J. Biol. Chem. 271:12859-2866) identified G545as an Arabidopsis cDNA (STZ), which increases the tolerance of yeast toLi+ and Na+. They found that STZ expression is most abundant in leavesand roots, and that its level of expression increases slightly uponexposure of the plant to salt. The second group (Meissner and Michael(1997) Plant Mol. Biol. 33:615-624), identified G545 (ZAT10) in a groupof Arabidopsis C2H2 zinc finger protein-encoding cDNAs that theyisolated by degenerate PCR. According to their data, ZAT10 is expressedin roots, shoots and stems. G545 and closely-related clade membersequences each comprise a conserved C2H2 DNA-binding zinc finger domainthat is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

Plants overexpressing G545 were smaller than wild type plants, floweredearly, and in extreme cases were infertile. G545 overexpressionconferred tolerance to phosphate deficiency. However, the small size ofthe seedlings made it difficult to make root growth comparisons withwild type. 35S::G545 lines also appeared more sensitive to NaCl thanwild type plants. Finally, G545 overexpressing plants appeared to besignificantly more susceptible to pathogens than control plants.

We have now analyzed the function of G545 by characterizing 35S:G545overexpressing lines in a C/N sensing assay. Anthocyanin accumulationwas elevated compared to control wild-type seedlings (Table 14). Thus,the gene could have a role in the response to nutrient limitation orabiotic stress.

Utilities.

The first useful phenotype G545 overexpressors are displaying is theirtolerance to phosphate deficiency. Young plants have a rapid intake ofphosphorous, so it is important that seed beds have high enough contentin phosphate to sustain their growth. Also, root crops such as carrot,potato and parsnip will all decrease in yield if there is insufficientphosphate available. Phosphate costs represent a relatively small butsignificant portion of farmers' operating costs (3-4% of total costs toa corn farmer in the US, higher to a vegetable grower). Plants that aretolerant to phosphate deficiency can represent a cost saving forfarmers, especially in areas where soils are very poor in phosphate.

Another desirable phenotype, salt tolerance, may arise from G545silencing rather than overexpression. Additionally, G545 appears to beinduced by cold, drought, salt and osmotic stresses, which is inagreement with a potential role of the genes in protecting the plant insuch adverse environmental conditions.

G545 appears to be involved in the control of defense processes.However, overexpression of G545 made Arabidopsis plants more susceptibleto disease. This negative effect will have to be corrected before G545can be used in a crop to induce tolerance to low phosphate. One exampleof a method to approach the problem would be to restrict overexpressionof G545 to roots.

These assays indicate that G545 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G760 Clade of Transcription Factor Polypeptides G760 (SEQ ID NO: 427and 428)

G760 corresponds to the gene NAC2, GenBank accession no. AF201456. G760was found to be highly expressed in root meristems. G760 andclosely-related clade member sequences each comprise a conserved NACdomain that is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR analysis demonstrated that G760 was uniformly expressed in alltissues and under all conditions. The function of G760 gene was analyzedusing transgenic plants in which the gene was expressed under thecontrol of the 35S promoter. Many 35S::G760 primary transformants weresmall and had rather curled, twisted, leaves. However, T2 populationsall showed a wild-type phenotype, indicating that activity of thetransgene might have been reduced between the generations. In addition,overexpression of G760 in Arabidopsis resulted in T2 seedlings that werehypersensitive to growth on ACC.

We have now analyzed the function of G760 by characterizing 35S:G760overexpressing lines in a C/N sensing assay. Anthocyanin accumulationwas greatly elevated compared to that observed in control wild-typeseedlings in one of three lines tested (Table 14). Thus, G760 could havea role in response to low nutrient conditions.

Utilities.

G760 could be used to manipulate ethylene signal transduction orresponse pathways. The gene could be used to manipulate the processesinfluenced by ethylene, such as fruit ripening.

These assays indicate that G760 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G773 Clade of Transcription Factor Polypeptides G773 (SEQ ID NO: 429and 430)

G773 (AT3G15500) in the sequence of GenBank accession number AB022218,released by the Arabidopsis Genome Initiative and corresponds to AtNAC3(Takada et al. (2001) Development 128:1127-1135). G773 andclosely-related clade member sequences each comprise a conserved NACdomain that is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR analysis determined that G773 has the highest levels ofexpression in roots, flowers and embryos and is expressed at medium orlow levels in rosettes, siliques and seedlings. RT-PCR data alsoindicated a significant induction of G773 transcripts accumulation uponauxin, heat, osmotic, drought and Fusarium treatments. The phenotype ofthe transgenic lines analyzed was wild type in all assays performed atthat time.

We have now analyzed the function of G773 by characterizing 35S::G773overexpressing lines in a C/N sensing assay. Anthocyanin accumulationwas elevated compared to that observed in wild-type seedlings (Table14). Thus, G773 could have a role in the response to nutrient limitation

Utilities.

These assays indicate that G773 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G937 Clade of Transcription Factor Polypeptides G937 (SEQ ID NO: 431and 432)

G937 (AT1G49560) was initially identified in the sequence of BAC F14J22(GenBank accession AC011807) released by the Arabidopsis GenomeInitiative. G937 and closely-related clade member sequences eachcomprise a conserved GARP DNA-binding domain that is expected tofunction in a similar manner in each of these related sequences, thatis, by playing a central role in transcriptional regulation and in theconferring of shared traits.

Experimental Observations.

RT-PCR expression analysis demonstrated that G937 was expressed atrelatively high levels throughout the plant, and was not induced by anycondition tested. The function of this gene was analyzed usingtransgenic plants in which G937 was expressed under the control of the35S promoter. The majority of 35S::G937 primary transformants weresmaller than wild type, slightly slow developing, and produced thininflorescence stems that carried relatively few siliques.

We have now analyzed 35S::G937 seedlings in a C/N sensing assay.Anthocyanin accumulation was less than that observed in controlwild-type seedlings in one of three lines tested (Table 14). Thus, G937might have a role in the response to nutrient limitation

Utilities.

G937 may be useful for regulation of plant growth and development.

These assays indicate that G937 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G971 Clade of Transcription Factor Polypeptides G971 (SEQ ID NO: 433and 434)

G971 (AT3G54990) corresponds to gene F28P10.30 (GenBank accessionCAB41085). G971 and closely-related clade member sequences each comprisea conserved AP2 DNA-binding domain that is expected to function in asimilar manner in each of these related sequences, that is, by playing acentral role in transcriptional regulation and in the conferring ofshared traits.

Experimental Observations.

RT-PCR expression analysis indicated that G971 is ubiquitouslyexpressed. The function of G971 was studied using transgenic plants inwhich the gene was expressed under the control of the 35S promoter.Overexpression of G971 produced a marked delay in the transition toflowering. No obvious phenotype was observed during that period with35S::G971 plants in physiological assays.

We have now analyzed the function of G971 by characterizing 35S:G971overexpressing lines in a C/N sensing assay. Anthocyanin accumulationwas elevated compared to the levels seen in control wild-type seedlings(Table 14). Thus, G971 could have a role in the response to low nitrogenconditions.

Utilities.

G971 could be used to modify flowering time characteristics.

These assays indicate that G971 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G988 Clade of Transcription Factor Polypeptides G988 (SEQ ID NO: 435and 436)

G988 (AT1G55580) corresponds to a protein annotated as hypothetical inBAC F20N2 (GenBank accession number AC002328) from chromosome 1 ofArabidopsis. The sequence for G988 is described in patent application WO9846759. G988 and closely-related clade member sequences each comprise aconserved SCR domain that is expected to function in a similar manner ineach of these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR expression analysis indicated that G988 appears to be expressedprimarily in flower and silique tissue and is induced in response toheat treatment. The function of this gene was analyzed using transgenicplants in which G988 was expressed under the control of the 35Spromoter. Plants overexpressing G988 had multiple morphologicalphenotypes. The transgenic plants were generally smaller than wild-typeplants, had altered leaf, inflorescence and flower development, alteredplant architecture, and altered vasculature.

We have now analyzed the function of G988 by characterizing 35S::G988overexpressing lines in a C/N sensing assay. Anthocyanin accumulationwas elevated compared to that observed in control wild-type seedlings(Table 14). Thus, G988 could have a role in the response to low nitrogenconditions.

Utilities.

Based on the observed morphological phenotypes of the transgenic plants,it is possible that G988 could be used to create plants with largerflowers. This could have potential value in the ornamental horticultureindustry. The reduction in the formation of lateral branches indicatesthat G988 could have possible utility on the forestry industry. TheArabidopsis plants overexpressing G988 also had reduced fertility. Thiscould actually be a desirable trait in some instances, as it could beexploited to prevent or minimize the escape of GMO pollen into theenvironment.

These assays indicate that G988 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G989 Clade of Transcription Factor Polypeptides G989 (SEQ ID NO: 437and 438)

G989 (AT5G41920) corresponds to a predicted SCARECROW generegulator-like protein in annotated P1 clone (GenBank accessionAB017067). G989 and closely-related clade member sequences each comprisea conserved SCR domain that is expected to function in a similar mannerin each of these related sequences, that is, by playing a central rolein transcriptional regulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR expression analysis indicated that G989 appeared to be expressedat highest levels in embryo tissue, and at low levels in all othertissues tested. Expression of G989 appeared to be induced in response totreatment with auxin, ABA, heat and drought, and to a lesser extent inresponse to salt treatment and osmotic stress. The function of this genewas also analyzed using transgenic plants in which G989 was expressedunder the control of the 35S promoter. Plants overexpressing G989appeared to be somewhat early flowering, but in other respects appearednormal, and showed a wild-type response in the physiological assaysperformed at that time.

We have now analyzed 35S::G989 seedlings in a C/N sensing assay.Anthocyanin accumulation was slightly less than that observed in controlwild-type seedlings (Table 14), indicating that G989 has a role in theresponse to nutrient limitation.

Utilities.

If the early flowering phenotype is reproducible in a larger number ofplants and under a wider range of environmental conditions, it ispossible that G989 could be used to alter flowering time in other plantspecies. A number of Arabidopsis genes have already been shown toaccelerate flowering when constitutively expressed. These include LEAFY,APETALA1 and CONSTANS. In these cases, however, the early floweringplants showed undesirable side effects such as extreme dwarfing,infertility, or premature termination of shoot meristem growth (Mandeland Yanofsky (1995) Nature 377: 522-524, Weigel and Nilsson (1995)Nature 377: 495-500, Simon et al. (1996). 384: Nature 59-62). Ourinitial study indicates that G989 can induce flowering without thesetoxic pleiotropic effects.

These assays indicate that G989 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G1073 Clade of Transcription Factor Polypeptides G1069 (SEQ ID NO:239 and 240)

G1069 is a paralog of G1073 from Arabidopsis. G1069 corresponds toAT4G14465 and is a member of the AT-Hook related proteins inArabidopsis. G1069 and closely-related clade member sequences eachcomprise a conserved At-hook domain and a second conserved domain (aminoacids 76-218) or the DUF296 domain (amino acids 93-211) that areexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

G1069 was predominantly expressed in roots, based our initial analysisof RT-PCR results. The function of G1069 was analyzed using transgenicplants in which G1069 was expressed under the control of the 35Spromoter. Plants overexpressing G1069 showed changes in leafarchitecture, reduced overall plant size, and retarded progressionthrough the life cycle. One G1069 overexpressing line showed moretolerance to abiotic stress when they were germinated in high sucroseplates. This line (line 41) also showed insensitivity to ABA in agermination assay. Moreover, seedlings of this line also look smallerand chlorotic in control germination plates.

We have now analyzed 35S::G1069 seedlings in a C/N sensing assay.Anthocyanin accumulation was slightly less than that observed in controlwild-type seedlings in one line (line 41) (Table 14), indicating thatoverexpression of G1069 in Arabidopsis gave a very mild response inovercoming the stress caused by this assay. The other two lines werewild type. Line 41 also gave a positive stress phenotype when germinatedon media containing sucrose and ABA.

Utilities.

Because of its effect on leaf architecture, plant size and plantdevelopment, G1069 may have some utility in modifying plant growth anddevelopment. In addition, the promoter of G1069 may have some utility asa promoter that is active in roots.

These assays indicate that G1069 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

G2789 (SEQ ID NO: 247 and 248)

The sequence of G2789 (AT3G60870) was obtained from the Arabidopsisgenomic sequencing project, GenBank accession number AL162295, based onits sequence similarity to other AT-hook related proteins. G2789 is asequence functionally and structurally related to G1073 fromArabidopsis. G2789 and closely-related clade member sequences eachcomprise a conserved At-hook domain and a second conserved domain (aminoacids 68-208) or the DUF296 domain (amino acids 86-201) that areexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR analysis indicated that G2789 is expressed at moderate levels inroots, flowers, embryos, siliques, and germinating seeds. At this time,G2789 function was analyzed using 35S::G2789 lines. Overexpression ofG2789 in Arabidopsis resulted in seedlings that were ABA insensitive andabiotic stress tolerant. Overexpression of G2789 also producedalterations in leaf and flower development, and caused severe reductionsin fertility. 35S::G2789 primary transformants displayed a variety ofleaf abnormalities including; leaf curling, serrations, and changes inleaf shape and area.

We have now analyzed 35S::G2789 seedlings in a C/N sensing assay.Anthocyanin accumulation was significantly less than that observed incontrol wild-type seedlings (Table 14). Thus, the gene might have a rolein nutrient limitation responses. However, because the C/N sensing assayhas high levels of sucrose, the enhanced vigor of seedlings seen in thisassay could be related to the enhanced abiotic stress previouslyobserved. It remains to be determined whether the effects seen in thisassay are related to the apparent involvement of the gene in shadetolerance

Utilities.

G2789 could be used to alter a plant's response to water deficitconditions and therefore, could be used to engineer plants with enhancedtolerance to drought, salt stress, and freezing.

These assays also indicate that G2789 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G1090 Clade of Transcription Factor Polypeptides G1090 (SEQ ID NO:439 and 440)

Experimental Observations.

In a C/N sensing assay anthocyanin accumulation was slightly less inG1090 seedlings than that observed in control wild-type seedlings in oneof three lines tested (Table 14), indicating that overexpression ofG1090 in Arabidopsis gives a mild response in overcoming the stresscaused by this assay. G1090 and closely-related clade member sequenceseach comprise a conserved AP2 DNA binding domain that is expected tofunction in a similar manner in each of these related sequences, thatis, by playing a central role in transcriptional regulation and in theconferring of shared traits.

Utilities.

These assays indicate that G1090 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G1322 Clade of Transcription Factor Polypeptides G1322 (SEQ ID NO:441 and 442)

G1322 is a member of the (R1)R2R3 subfamily of myb transcriptionfactors. G1322 corresponds to Myb57, a gene identified by Kranz et al.(1998) Plant J. 16: 263-276). The authors used a reverse-Northern blottechnique to study the expression of this gene in a variety of tissuesand under a variety of environmental conditions. They were unable todetect the expression of G1322 in any tissue or treatments tested (Kranzet al (1998) supra). G1322 and closely-related clade member sequenceseach comprise a conserved MYB_related DNA-binding domain that isexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR analysis indicated that G1322 is expressed primarily in flowertissue and is not induced in response to any environmentalstress-related condition tested. At that time, the function of G1322 wasanalyzed using transgenic plants in which the gene was expressed underthe control of the 35S promoter. 35S::G1322 transgenic plants hadchanges in overall plant size and leaf development. 35S::G1322 plantswere distinctly smaller than controls and developed curled dark-greenleaves. Following the switch to flowering, the plants formed relativelythin inflorescence stems and had a rather poor seed yield. In addition,overexpression of G1322 resulted in plants with an altered etiolationresponse as well as enhanced tolerance to germination under chillingconditions.

We have now analyzed 35S::G1322 seedlings in a C/N sensing assay.Anthocyanin accumulation was significantly less than that observed incontrol wild-type seedlings in one of three lines examined (Table 14),indicating that the gene may play a role in the response to low nutrientconditions.

Utilities.

The potential utilities of G1322 include altering a plant's chillingsensitivity and altering a plant's light response.

These assays indicate that G1322 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G1587 Clade of Transcription Factor Polypeptides G1587 (SEQ ID NO:443 and 444)

G1587 (AT2G01500) was originally identified as a novel homeobox genewithin BAC F2I9 (GenBank accession AC005560). G1587 and closely-relatedclade member sequences each comprise a conserved homeobox domain that isexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR experiments revealed that the gene is predominantly expressed inflowers. At that time, the function of G1587 was assessed by analysis oftransgenic Arabidopsis lines in which the cDNA was constitutivelyexpressed from the 35S CaMV promoter. However, overexpression of G1587produced deleterious effects on growth and development. The mostseverely affected 35S::G1587 primary transformants died at very earlystages of development. Other seedlings, however, displayed rathercontorted cotyledons, long hypocotyls, and produced small narrow darkgreen leaves. Following the switch to flowering, such plants formedrather thin inflorescence stems that carried somewhat small numbers offlowers. Floral organs were often contorted or poorly developed, and asa result, seed yield was poor. The three lines used for physiologicalanalysis showed a relatively weak phenotype.

We have now analyzed 35S::G1587 seedlings in a C/N sensing assay.Anthocyanin accumulation was slightly less than that observed in controlwild-type seedlings in all three of the lines examined (Table 14),indicating that the gene may play a role in the response to low nutrientconditions.

Utilities.

The RT-PCR data indicates that the G1587 promoter might be of utilityfor driving expression of transgenes within flowers. Additionally, iffuture studies confirm that G1587 has a function in the regulation offlower development, the gene might be used to manipulate thosestructures.

These assays indicate that G1587 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G1666 Clade of Transcription Factor Polypeptides G1666 (SEQ ID NO:445 and 446)

The sequence of G1666 was obtained from the Arabidopsis genomesequencing project, GenBank accession number AL049482, based on itssequence similarity within the conserved domain to other HLH/MYC relatedproteins in Arabidopsis. G1666 has been recently identified as TT8 froma T-DNA mutagenized Arabidopsis collection (Nesi et al. (2000) PlantCell. 12:1863-1878). G1666 and closely-related clade member sequenceseach comprise a conserved HLH DNA-binding and dimerization domain thatis expected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

It has been shown that G1666/TT8 is involved in the regulation offlavonoid biosynthesis in the Arabidopsis seed coat. The protein isrequired for normal expression of two flavonoid biosynthetic genes, DFRand BAN. G1666 transcripts accumulate more in developing siliques and inyoung seedlings compared to other tissues.

Experimental Observations,

RT-PCR expression analysis indicated that G1666 was predominantlyexpressed in reproductive tissue such as embryo, siliques and flowers.At that time, the function of G1666 was analyzed using a line homozygousfor a T-DNA insertion in the gene and transgenic plants in which thegene was expressed under the control of the 35S promoter. Plantshomozygous for a T-DNA insertion within G1666 produced yellow seed.However, at all other developmental stages, these plants appeared wildtype. G1666 knockout mutant seedlings responded differently in anethylene insensitivity assay compared to the wild-type controls.Seedlings germinated in the dark on ACC-containing media are moreseverely stunted than the wild-type controls. 35S::G1666 plants werewild type in all assays performed.

We have now analyzed the function of G1666 by characterizing a linehomozygous for a T-DNA insertion in G1666 in a C/N sensing assay.Anthocyanin accumulation was slightly less than that observed in controlwild-type seedlings in knocked-out G1666 lines (Table 14), indicatingthat the gene might have a role in the response to nutrient limitation.However the lack of anthocyanin production observed in this assay couldbe related to the block in flavonoid biosynthesis caused by the T-DNAinsertion within G1666.

Utilities.

Because expression of G1666 is flower, embryo and silique specific, itspromoter could be useful for targeted gene expression in these organs.

Co-overexpression of G1666 with G669, and G663 could be used to increasethe production of flavonoid compounds, including anthocyanins andcondensed tannins, in Arabidopsis. The potential utilities of this geneinclude alterations in pigment production for horticultural purposes,and possibly increasing stress resistance in combination with anothertranscription factor. Flavonoids have antimicrobial activity and couldbe used to engineer pathogen resistance. Several flavonoid compoundshave health promoting effects such as the inhibition of tumor growth andcancer, prevention of bone loss and the prevention of the oxidation oflipids. Increasing levels of condensed tannins, whose biosyntheticpathway is shared with anthocyanin biosynthesis, in forage legumes is animportant agronomic trait because they prevent pasture bloat bycollapsing protein foams within the rumen.

These assays indicate that G1666 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G1700 Clade of Transcription Factor Polypeptides G1700 (SEQ ID NO:447 and 448)

G1700 (AT4G10150), a member of the RING C3H2C3 gene family, wasidentified in the sequence of BAC T9A4 (GenBank accession AF096373),released by the Arabidopsis Genome Initiative. G1700 and closely-relatedclade member sequences each comprise a conserved homeobox and RINGfinger domain that is expected to function in a similar manner in eachof these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR expression analysis indicated that G1700 was highly expressed inembryos. No expression in any other tissue was detected at that time. Aline homozygous for a T-DNA insertion in G1700 was used to determine thefunction of this gene. The phenotype of G1700 knock-out plants was wildtype in all assays performed.

We have now analyzed the function of G1700 by characterizing a linehomozygous for a T-DNA insertion in G1700 in a C/N sensing assay.Anthocyanin accumulation was slightly less than that observed in controlwild-type seedlings (Table 14), indicating that the gene might have arole in the response to low nutrient conditions.

Utilities.

The strong expression in embryos indicates that the promoter of G1700could be used to drive embryo specific expression.

These assays indicate that G1700 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

HAP5 Transcription Factor Polypeptides G1818 (SEQ ID NO: 449 and 450)

G1818 (AT5G50490), a member of the Hap5-like subfamily of CCAAT-boxbinding transcription factors, was identified in the sequence of P1clone MBA10 (GenBank accession AB025619). G1818 and closely-relatedclade member sequences each comprise a conserved CCAAT binding factordomain that is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR expression analysis indicated that G1818 expression was detectedin embryos, flowers and siliques. Expression of G1818 could also bedetected in leaf tissue following cold and auxin treatments. At thattime, the function of this gene was analyzed using transgenic plants inwhich G1818 was expressed under the control of the 35S promoter. Withthe exception of delayed flowering and subtle changes in leaf morphology(flatter leaves), the phenotype of these transgenic plants was wild-typein all assays performed.

We have now analyzed 35S::G1818 seedlings in a C/N sensing assay.Anthocyanin accumulation was substantially lower than that observed incontrol wild-type seedlings (Table 14), indicating that G1818 plays arole in the response to low nutrient conditions.

Utilities.

G1818 could be used to delay flowering in plants, which may extendvegetative development and bring about larger yields.

These assays indicate that G1818 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G1868 Clade of Transcription Factor Polypeptides G1868 (SEQ ID NO:451 and 452)

G1868 (AT4G37740) was found in the sequence of BAC clone T28119 (GenBankaccession AL035709) based on its amino acid sequence similarity to therice Growth-regulating-factor1 (GRF1). G1868 and closely-related clademember sequences each comprise a QRQ and WRC conserved domain that areexpected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR expression analysis revealed a constitutive expression in alltissues except roots. At this time, the function of G1868 was analyzedthrough its ectopic overexpression in plants. No apparent changes wereapparent when compared to control plants.

We have now analyzed 35S::G1868 seedlings in a C/N sensing assay.Anthocyanin accumulation was slightly less than that observed in controlwild-type seedlings in two lines (Table 14), indicating that G1868 mighthave a minor role in the response to low nutrient conditions.

Utilities.

These assays indicate that G1868 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G1888 Clade of Transcription Factor Polypeptides G1888 (SEQ ID NO:453 and 454)

G1888 (AT4G39070) was identified in the sequence of BAC accession numberAL035679, released by the Arabidopsis Genome Initiative and is a memberof the Z-CO-like transcription factor family. G1888 and closely-relatedclade member sequences each comprise at least one conserved B-Box-typezinc finger domain that is expected to function in a similar manner ineach of these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Observations.

G1888 was found to be constitutively expressed in all tissues andenvironmental conditions tested based on RT-PCR expression analysis. Thefunction of this gene was analyzed using transgenic plants in whichG1888 was expressed under the control of the 35S promoter at that time.Overexpression of G1888 produced plants with dark green leaves, markedlyslowed development (bolting and senescing late), and reduced overallplant size. When grown on MS agar plates, increased leaf anthocyaninlevels and chlorosis were noted.

We have now analyzed the function of G1888 by characterizing 35S:G1888overexpressing lines in a C/N sensing assay. Anthocyanin accumulationwas strikingly elevated compared to that observed in control wild-typeseedlings (Table 14). It should be noted that the higher levels ofanthocyanin seen in these assays could be related to the generallydarker coloration of 35S::G1888 lines that we observed previously. It isinteresting that the gene is most closely related to G1482, which alsocauses elevation of anthocyanin levels in seedlings when overexpressed.Thus, this pair of genes might represent transcriptional regulators ofthe phenylpropanoid pathway and as such might be used to impact avariety of additional traits such as disease responses, lignincomposition, and nutritional quality.

Utilities.

These assays indicate that G1888 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G2117 Clade of Transcription Factor Polypeptides G2117 (SEQ ID NO:455 and 456)

G2117 (AT1G68880) was identified in the sequence of BAC T6L1 (GenBankaccession AC011665) released by the Arabidopsis Genome Initiative and isa member of the bZIP transcription factor family. It has also beendescribed as AtbZIP8 (GenBank accession number AF400621). G2117 andclosely-related clade member sequences each comprise a conserved basicregion leucin zipper (bZIP) domain that is expected to function in asimilar manner in each of these related sequences, that is, by playing acentral role in transcriptional regulation and in the conferring ofshared traits.

Experimental Observations.

RT-PCR expression analysis indicated that G2117 was highly expressed inroots compared to all other tissues tested. The function of G2117 wasanalyzed using transgenic plants in which the gene was expressed underthe control of the 35S promoter. Plants overexpressing G2117 had alteredleaf morphology, coloration, and smaller overall plant size and weregenerally small with short, rounded, dark green leaves that becamecurled later in development. These plants generated thin inflorescencestems developed a rather bushy appearance, and had reduced fertility.

We have now analyzed the function of G2117 by characterizing 35S:G2117overexpressing lines in a C/N sensing assay. Anthocyanin accumulationwas elevated compared to the levels observed in control wild-typeseedlings (Table 14). Thus, G2117 could have a role in the response tonutrient limitation. However, given that increased anthocyanin levelswere seen on control plates, the phenotype is possibly an aspect ofdarker coloration seen in these lines, rather than an indicator of a C/Nsensing response.

Utilities.

These assays indicate that G2117 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G2131 Clade of Transcription Factor Polypeptides G2131 (SEQ ID NO:457 and 458)

G2131 (AT1G79700) corresponds to gene F20B17.12 (GenBank accessionAAF68121) and is a member of the AP2 transcription factor family. G2131and closely-related clade member sequences each comprise a conserved AP2DNA binding domain that is expected to function in a similar manner ineach of these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits. G2131and closely-related clade member sequences each comprise a conserveddomain that is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR expression analysis indicated that G2131 is ubiquitouslyexpressed and was not significantly induced by any of the environmentalconditions tested. At that time, the function of G2131 was studied usingtransgenic plants in which the gene was expressed under the control ofthe 35S promoter. 35S::G2131 plants did not show consistent alterationsin morphology and development, and were essentially wild type in thephysiological analyses that were performed.

G2131 overexpressing plants showed elevated levels of campesterol inleaves.

We have now analyzed 35S::G2131 seedlings in a C/N sensing assay.Anthocyanin accumulation was significantly less than that observed incontrol wild-type seedlings (Table 14). Thus, this gene is indicated ashaving a role in responses to nutrient limitation.

Utilities.

Phytosterols are an important source of precursors for the manufactureof human steroid hormones by semisynthesis. Sitosterols andstigmasterols, not campesterol, are the preferred sources from seedcrops. However, it is conceivable that proper regulation of G2131expression or activity could lead to elevated levels of the importanthuman steroid precursors. Phytosterols and their hydrogenatedderivatives phytostanols also have proven cholesterol-loweringproperties. However, it is unclear what the relative efficacies ofsitosterol and campesterol are for lowering blood cholesterol levels. IfG2131 could be used to increase total phytosterol levels in leaves, itwould be very useful for both types of applications.

These assays indicate that G2131 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

The G2520 Clade of Transcription Factor Polypeptides G2520 (SEQ ID NO:459 and 460)

The sequence of G2520 (AT1G59640) was originally obtained fromArabidopsis genomic sequencing project, GenBank accession numberAC009317, based on its sequence similarity within the conserved domainto other bHLH related proteins. G2520 and closely-related clade membersequences each comprise a conserved HLH DNA-binding and dimerizationdomain that is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

RT-PCR expression analysis indicated that G2520 was expressedubiquitously. At that time, the function of G2520 was analyzed usingtransgenic plants in which G2520 was expressed under the control of the35S promoter. At early stages, 35S::G2520 transformants displayedabnormal curled cotyledons, long hypocotyls, and rather short roots.During the vegetative phase, these plants were formed somewhat smallflat leaves. Following the switch to reproductive growth, 35S::G2520inflorescences were typically very spindly, slightly pale colored, andstems often split open at late stages. Flowers were frequently smallwith narrow organs and showed poor pollen production. Because of thesedefects, seed yield from 35S::G2520 plants was low compared to wild-typecontrols.

We have now analyzed 35S::G2520 seedlings in a C/N sensing assay.Anthocyanin accumulation was significantly less than that observed incontrol wild-type seedlings (Table 14), indicating that this gene mighthave a role in the response to nutrient limitation.

Interestingly, we previously observed that overexpression lines showedlight response phenotypes such as long hypocotyls, and a pale coloration(reduced levels of pigmentation). However, it remains to be determinedwhether the response to low nutrient conditions is related to theseeffects. However, it is interesting compare the strikingly similareffects on pigment production observed between 35S::G2520 lines andoverexpression lines from the G682 subclade reports. Given that genesfrom the MYB family are in some cases known to have partners in theHLH/MYC family, it is possible that the G2520 might act in the samepathway.

Utilities.

In addition to the observed shade avoidance phenotype, these assaysindicate that G2520 and its equivalogs are potential regulators of aplant's response to low nutrient conditions. For further analysis, seethe discussion above: “Potential Applications of Polynucleotides andPolypeptides that Regulate C/N sensing”.

The G2522 Clade of Transcription Factor Polypeptides G2522 (SEQ ID NO:461 and 462)

The sequence of G2522 (AT3G61310) was initially obtained from theArabidopsis genomic sequencing project (GenBank accession AL137898)based on its sequence similarity within the conserved domain to otherAT-hook related proteins. G2522 and closely-related clade membersequences each comprise a conserved domain that is expected to functionin a similar manner in each of these related sequences, that is, byplaying a central role in transcriptional regulation and in theconferring of shared traits. G2522 and closely-related clade membersequences each comprise a conserved At-hook domain and a secondconserved domain (amino acids 143-291) or the DUF296 domain (amino acids164-284) that are expected to function in a similar manner in each ofthese related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits

Experimental Observations.

RT-PCR expression analysis indicated that G2522 is expressed at moderatelevels in flowers, embryos, and siliques, and is found at significantlylower levels throughout the rest of the plant. The gene was notsignificantly induced by any environmental condition tested. Thefunction of G2522 was also analyzed using transgenic plants in whichG2522 was expressed under the control of the 35S promoter.Overexpression of G2522 did not produce any consistent phenotypicalteration in any assay performed when compared to wild-type controlplants.

We have now analyzed 35S::G2522 seedlings in a C/N sensing assay.Anthocyanin accumulation was slightly less than that observed in controlwild-type seedlings (Table 14), indicating that the gene might have arole in the response to low nutrient conditions.

Utilities.

These assays indicate that G2522 and its equivalogs are potentialregulators of a plant's response to low nutrient conditions. For furtheranalysis, see the discussion above: “Potential Applications ofPolynucleotides and Polypeptides that Regulate C/N sensing”.

Table 14 lists the results obtained with transgenic seedlings germinatedon two different media for the purpose of differentiating plants withaltered C/N sensing. The first column lists the Gene IdentificationNumber (GID), the second column identifies the gene family of thecorresponding sequence, the third column identifies whether the gene wasoverexpressed or knocked out, and the fourth and fifth columns list theresults obtained with high sucrose media lacking a nitrogen source andhigh sucrose media with glutamine as a nitrogen source, respectively.Generally, increased tolerance was measured as lower anthocyaninaccumulation than controls, and increased sensitivity as greateranthocyanin accumulation than controls. The plants' responses as theyappear in the fourth and fifth columns were given one of four scores:

++ markedly enhanced tolerance;

+ mild/moderately enhanced tolerance;

wt comparable tolerance to wild-type controls, and

− mild to moderately increased sensitivity.

TABLE 14 Sequences identified as modifying the response to nutrientlimitation in C/N sensing assays Response of Response of transgenictransgenic plants on high plants on high sucrose without sucrose plusGID Gene family OE/KO a nitrogen source glutamine G24 AP2 OE + + G154MADS OE + + CPC MYB-related OE ++ ++ G226 MYB-related OE ++ ++ G384 HBOE − − G486 CAAT OE + + G545 Z-C2H2 OE − − G682 MYB-related OE ++ + G760NAC OE − − G773 NAC OE − − G937 GARP OE + + G971 AP2 OE − − G988 SCR OE− − G989 SCR OE + + G1069 AT-hook OE + + G1090 AP2 OE + + G1322MYB-(R1)R2R3 OE ++ ++ G1587 HB OE + + G1666 HLH/MYC KO + + G1700RING/C3H2C3 KO + + G1816 MYB-related OE ++ + G1818 CAAT OE + + G1868GRF-like OE + + G1888 Z-CO-like OE − − G2117 bZIP OE − − G2131 AP2 OE ++++ G2520 HLH/MYC OE ++ ++ G2522 AT-hook OE + + G2718 MYB-related OE ++ +G2789 AT-hook OE ++ ++ G8 AP2 OE − − G27 AP2 OE wt − G156 MADS OE + +G161 MADS OE − − G168 MADS OE − wt G183 WRKY OE + + G189 WRKY OE + +G200 MYB-(R1)R2R3 KO − − G234 MYB-(R1)R2R3 OE + + G237 MYB-(R1)R2R3OE + + G275 AKR OE + + G326 Z-CO-like OE − − G347 Z-LSD-like OE wt +G427 HB OE + + G505 NAC OE − − G590 HLH/MYC OE + + G602 DBP OE + + G618TEO OE + + G635 TH OE + + G643 TH OE + + G653 Z-LIM OE + + G657MYB-(R1)R2R3 OE wt + G837 AKR OE wt + G866 WRKY OE + + G872 AP2 OE + +G904 RING/C3H2C3 OE + + G912 AP2 OE + + G932 MYB-(R1)R2R3 OE wt + G958NAC OE + wt G964 HB KO ++ + G975 AP2 OE + + G979 AP2 OE wt + G1049 bZIPOE + + G1246 MYB-(R1)R2R3 OE + + G1255 Z-CO-like OE + + G1266 AP2 OEwt + G1331 MYB-(R1)R2R3 OE + + G1332 MYB-(R1)R2R3 OE + + G1494 HLH/MYCOE + + G1535 HB KO wt + G1649 HLH/MYC OE + + G1750 AP2 OE + + G1773RING/C3HC4 KO + + G1835 GATA/Zn OE wt − G1930 AP2 OE + + G2053 NAC OEwt + G2057 TEO OE + + G2133 AP2 OE wt + G2144 HLH/MYC OE + + G2145HLH/MYC OE + + G2295 MADS OE + + G2512 AP2 OE + + G2531 NAC OE + wtG2535 NAC OE − − G2590 MADS OE + + G2719 MYB-(R1)R2R3 OE + + G1792 AP2OE + + Abbreviations and symbols: wt wild-type response + increasedgrowth and/or vigor relative to wild-type − decreased growth and/orvigor relative to wild-type

Example X: Results of Shade Tolerance Assays

This example provides experimental evidence for increased shadetolerance controlled by transcription factor polypeptides andpolypeptides of the invention.

The twelve shade avoidance-inducing sequences that were most extensivelyscrutinized spanned a range of diverse gene families: TH (G634), bZIP(G1048), RING/C3H2C3 (G1100), NAC (G1412, G2505), AP2 (G1796), Z-C2H2(G1995), HS (G2467), HB (G2550), SRS (G2640), WRKY (G2686), and AT-hook(G2789). Experimental data are provided for each of these sequences inExample VIII, but a number of the genes warrant special mention here.

G634 is of particular interest since we have determined that 35S::G634Arabidopsis lines also show enhanced drought tolerance in addition toshade tolerance. This gene could therefore confer yield savings viamultiple different traits.

The same ability to confer enhanced performance and yield by improvingmultiple traits is true for G2789. Overexpressors of G2789 were shown tobe insensitive to ABA, had altered carbon:nitrogen balance sensing (andthus overexpressors of this gene may thrive better than wild type underlow nutrient conditions), were osmotic stress tolerant, and recoveredbetter from drought than wild-type plants in a soil-based drought assay.

A G1412 homozygous T-DNA insertion mutant line for this gene showedshade tolerance. Thus, G1412 might be a target for obtaining shadetolerance via a non-transgenic strategy by screening for mutant lines ofcrops that carry a lesion within the ortholog(s) of G1412.

A number of the top lead genes, particularly G2550 and G2640, producedArabidopsis plants with a compact shoot morphology when overexpressed,which may represent a constitutive shade avoidance phenotype. Suchfeatures are similar to those seen in the high-yielding dwarf varietiesof cereals that facilitated the so-called “green revolution.” Theeffects of G2550 and G2640 overexpression on yield will be examined intarget crop species.

The G634 Clade of Transcription Factor Polypeptides G634 (SEQ ID NO: 231and 232)

G634 (AT1G33240) was initially identified as two public partial cDNAssequences (GTL1 and GTL2) which are splice variants of the same gene(Smalle et al. (1998) Proc. Natl. Acad. Sci. USA 95: 3318-3322). Thepublished expression pattern shows that G634 is highly expressed insiliques and not expressed in leaves, stems, flowers or roots. G634 andclosely-related clade member sequences each comprise at least oneconserved TH domain that is expected to function in a similar manner ineach of these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Observations.

Three constructs were initially made for G634: P324 (SEQ ID NO: 1015),P1374 (SEQ ID NO: 1013) and P1717 (SEQ ID NO: 1017). P324 was found toencode a shortened version of the G634 protein (SEQ ID NO: 1016). P1374and P1717 represent longer splice variants of G634 (SEQ ID NOs: 1014 and1018, respectively). Overexpression lines for P1717 were never analyzed.However lines for P324 showed some variable effects on size, butotherwise appeared normal. Plants overexpressing G634 had a dramaticincrease the density of trichomes. The trichomes were also larger insize than those of wild-type plants. The increase in trichome densitywas most noticeable on later arising rosette leaves, cauline leaves,inflorescence stems and sepals with the stem trichomes being more highlybranched than controls. Approximately half of the primary transformantsand two of three T2 lines showed the phenotype.

G634 overexpressing Arabidopsis lines did not exhibit a shade avoidancephenotype when grown under light deficient in the red region of thevisible spectrum; in experiments comparing 35S::G634 plants with wildtype controls, individual seedlings were examined after being grownunder light deficient in red wavelengths (b/FR). The G634 overexpressorsdid not exhibit a shade avoidance phenotype, as indicated by their shorthypocotyls produced under these conditions.

We recently tested lines for P324 and P1374 in a soil drought assay andfound that they showed an enhanced performance versus wild type; 6634overexpressors recovered from the effects of a drought treatmentsignificantly better than wild-type control plants. Additionally, ourrecent array experiments on plants undergoing a soil-drought experiment,indicated that G634 shows a small but significant up-regulationspecifically in the recovery phase, following re-watering at the end ofthe drought (see patent application Ser. No. 10/714,887).

Utilities.

We have now analyzed 35S::G634 lines (containing P1374, SEQ ID NO: 1013,which encodes SEQ ID NO: 1014) under white light versus light deficientin red wavelengths. All three lines tested did not exhibit a shadeavoidance phenotype under conditions where wild-type seedlings hadenhanced hypocotyl elongation.

The G1048 Clade of Transcription Factor Polypeptides G1048 (SEQ ID NO:807 and 808)

G1048 (AT1G42990) was initially identified as public partial EST T88194and in BAC F13A11 (GenBank accession AC068324) released by theArabidopsis Genome Initiative. G1048 and closely-related Glade membersequences each comprise a conserved basic region leucin zipper (bZIP)domain that is expected to function in a similar manner in each of theserelated sequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

During the genomics program, RT-PCR expression analysis indicated thatG1048 was constitutively expressed and not induced by any conditiontested. At that time, the function of G1048 was investigated byconstitutively expressing G1048 using the 35S promoter. Plantsoverexpressing G1048 were not significantly different to controls in anyassay performed.

G1048 overexpressing lines did not exhibit a shade avoidance phenotypewhen grown under light deficient in the red region of the visiblespectrum; individual seedlings grown on light deficient in redwavelengths (b/FR) were compared with wild-type control seedlings. Thiseffect was seen in two repeat experiments on a batch of mixed seed fromthree independent lines.

Utilities.

We have now analyzed 35S::G1048 lines grown under white light versuslight deficient in red light. A shade tolerance phenotype was observed,indicating that G1048 might be involved in the transcriptionalregulation of response to shade or light quality. As yet, though, thephenotype observed in a mixed batch of 35S::G1048 lines has not beenconfirmed by testing of individual lines. However, this gene was givenan “A” ranking because the phenotype seen in the screen on mixed lineswas moderately strong, and because G1048 is potentially related to HY5(Oyama et al. (1997) Genes Dev. 11:2983-2995), a gene that is wellestablished to be involved in light regulated development.

The G1100 Clade of Transcription Factor Polypeptides G1100 (SEQ ID NO:809 and 810)

G1100 was identified in the sequence of BACs T29F13, F1913 and T4C15based on its sequence similarity within the conserved domain to otherRING C3H2C3 related proteins in Arabidopsis. G1100 and closely-relatedclade member sequences each comprise a conserved RING finger domain thatis expected to function in a similar manner in each of these relatedsequences, that is, by playing a central role in transcriptionalregulation and in the conferring of shared traits.

Experimental Observations.

In our earlier genomics program, the function of G1100 was analyzed bydisrupting the gene with a T-DNA insertion. Homozygotes for thisinsertion appeared wild type in all assays performed. For the presentexperiments, the function of G1100 was studied using transgenic plantsin which the gene was expressed under the control of the 35S promoter.Overexpression of G1100 resulted in plants that were small, dark green,and slow developing. These effects were most prominent at later stages.Flowers were also small, had defects in organ formation and pollenproduction, and set few seeds. RT-PCR analysis indicated that G1100 isstrongly and specifically induced by drought and salicylic acid, and isnot detectable under normal conditions.

G1100 overexpressing lines did not exhibit a shade avoidance phenotypewhen grown under light deficient in red region of the visible spectrum;individual seedlings grown on light deficient in red wavelengths (b/FR)were compared with wild-type control seedlings. When the assay wasrepeated on individual lines, all three lines analyzed showed thephenotype. 35S::G1100 seedlings had short hypocotyls compared withwild-type seedlings.

Utilities.

We have now analyzed 35S::G1100 lines grown under white light ordeficient in red light. All three lines did not exhibit a shadeavoidance phenotype under conditions where wild-type seedlings hadenhanced hypocotyl elongation.

The G1412 Clade of Transcription Factor Polypeptides G1412 (SEQ ID NO:657 and 658)

G1412 is a member of the NAC family of transcription factors. G1412corresponds to gene At4g27410 and to sequence 1543 from Harper (2002)Patent Application WO 0216655-A. In this application, G1412 was reportedto be cold, osmotic and salt responsive in their microarray analysis (WO0216655-A). G1412 and closely-related clade member sequences eachcomprise a conserved NAC domain that is expected to function in asimilar manner in each of these related sequences, that is, by playing acentral role in transcriptional regulation and in the conferring ofshared traits.

Experimental Results.

In our original genomics screens, G1412 appeared to be constitutivelyexpressed in all tissues tested using RT-PCR analysis. Induction ofG1412 in leaf tissue was observed in response to ABA, heat, drought, andmannitol. This result was confirmed by microarray experiments, whichshowed that G1412 is induced by a variety of drought related treatments.

In our earlier studies, a T-DNA insertion mutant for G1412 was not shownto be morphologically different from wild type. 35S::G1412 transgenicplants showed normal morphology but were insensitive to ABA, and weresignificantly more tolerant to osmotic stress in a germination assay onmedia containing high concentrations of sucrose.

In our most recent experiments, T-DNA insertion mutants for G1412 didnot exhibit a shade avoidance phenotype when grown under light deficientin red region of the visible spectrum. Individual seedlings grown onlight deficient in red wavelengths (b/FR) were compared with wild-typecontrol seedlings; The G1412 knock-out seedlings had short hypocotylscompared with wild-type seedlings.

Utilities.

We have now analyzed KO.G1412 seedlings grown under white light versuslight deficient in the red wavelengths. KO.G1412 seedlings did notexhibit a shade avoidance phenotype under conditions where wild-typeseedlings had enhanced hypocotyl elongation. Thus, G1412 might berequired to mediate the shade avoidance response. However, 35S::G1412lines were not observed to show alterations in light-regulateddevelopment, suggesting that this gene is not sufficient to trigger ashade response.

The G1796 Clade of Transcription Factor Polypeptides G1796 (SEQ ID NO:811 and 812)

G1796 (At1g12980) is found in the sequence of GenBank accession numberAC007357. G1796 was identified by Banno et al. (Banno et al. (2001)Plant Cell 13: 2609-2618) as ESR1 (ENHANCER OF SHOOT REGENERATION) in ascreen for Arabidopsis cDNAs that could confer cytokinin-independentshoot formation from root cultures when overexpressed. G1796 was foundto be included in Patent Application W00200903. G1796 andclosely-related clade member sequences each comprise a conserved AP2DNA-binding domain that is expected to function in a similar manner ineach of these related sequences, that is, by playing a central role intranscriptional regulation and in the conferring of shared traits.

Experimental Results.

In our earlier genomics program, overexpression of G1796 was shown tocause growth defects: seedlings were generally small and formed darkcurled leaves. Portions of the flower and overall structure of theinflorescence were also affected. Flowers had poorly developed outerwhorl organs and formed thickened club-like carpels. RT-PCR expressionanalysis indicated that G1796 was expressed at low levels in root,flower and rosette, but not in stems, siliques, embryos or germinatingseeds.

Seedlings of overexpressing lines and wild-type controls were grown onlight deficient in red wavelengths (b/FR) and compared. Under theseconditions, the G1796 overexpressing lines did not exhibit a shadeavoidance phenotype.

Utilities.

We have now analyzed 35S::G1796 seedlings grown under white light orwhite light deficient in wavelengths corresponding to the red region ofthe visible spectrum. 35S::G1796 seedlings did not exhibit a shadeavoidance phenotype under conditions where wild-type seedlings hadenhanced hypocotyl elongation. This gene was given an “A” rankingbecause the phenotype seen in the screen on mixed lines was moderatelystrong.

35S::G1796 seedlings were also dark green in color compared to wildtype, confirming a result seen earlier in the earlier genomics program.

The G1995 Clade of Transcription Factor Polypeptides G1995 (SEQ ID NO:813 and 814)

G1995 (At3g58070) was identified in the sequence of BAC T10K17 (GenBankaccession number AL132977) based on its sequence similarity within theconserved domain to other Z-C2H2 related proteins in Arabidopsis. G1995and closely-related clade member sequences each comprise a conservedC2H2 DNA-binding zinc finger domain that is expected to function in asimilar manner in each of these related sequences, that is, by playing acentral role in transcriptional regulation and in the conferring ofshared traits.

Experimental Results.

The function of G1995 was studied using transgenic plants in which thegene was expressed under the control of the 35S promoter. Overexpressionof G1995 resulted in plants that were rather small, slow growing, andthat had flowers with increased trichome density on sepals and ectopictrichomes on carpels. The flowers also had rather poor pollen productionand many of the lines yielded only relatively small quantities of seed.Additionally a single extreme line displayed aerial rosette likestructures and had floral organs that were converted towards abract-like identity. Interestingly, in the strongest lines, the plantsfailed to undergo a clear transition to reproductive growth and formedleafy floral organs with vegetative characteristics. Thus, G1995 mightregulate this developmental transition.

In physiological analyses G1995 overexpressors showed size segregationand a slight increase in sensitivity to nutrient limitation.

Seedlings of overexpressing lines and wild-type controls were grown onlight deficient in red wavelengths (b/FR) and compared. Under theseconditions, the G1995 overexpressing lines did not exhibit a shadeavoidance phenotype.

Utilities.

We have now analyzed 35S::G1995 seedlings grown under white light orwhite light deficient in wavelengths corresponding to the red region ofthe visible spectrum. 35S::G1995 seedlings did not exhibit a shadeavoidance phenotype under conditions where wild-type seedlings hadenhanced hypocotyl elongation. Two out of three lines did not exhibit ashade avoidance phenotype.

It should be noted that G1995 is closely related to five other Z-C2H2genes we have previously analyzed: G370, G2826, G361, G362, and G2838,which produced broadly similar phenotypes when overexpressed, such asectopic trichomes on flowers, aerial rosettes, and various othermorphological defects. Importantly, these genes all produced a generalfailure in the vegetative to reproductive transition and showed floralorgans that were leaf-like. This effect, and the absence of hypocotylelongation seen in 35S::G1995 lines in this assay, could indicate thatthis group of TFs is involved in mediating a range of phytochromeregulated responses. However, we did not observe any effect on hypocotylelongation when these other Z-C2H2 overexpressing plants were examinedin our shade avoidance screen. Nevertheless, it should be noted that thelines were generally of very poor fertility and strongly affected linesset insufficient seed for inclusion in the shade tolerance assay (i.e.only lines with a relatively weak morphological phenotype could betested).

The G2467 Clade of Transcription Factor Polypeptides G2467 (SEQ ID NO:815 and 816)

G2467 is a member of the class-A heat shock transcription factor familycharacterized by an extended HR-A/B oligomerization domain. G2467 isfound in the sequence of the P1 clone MAA21 (GenBank accession AL163818)released by the Arabidopsis Genome Initiative. G2467 and closely-relatedclade member sequences each comprise a conserved HSF-type DNA-bindingdomain (or HS domain) that is expected to function in a similar mannerin each of these related sequences, that is, by playing a central rolein transcriptional regulation and in the conferring of shared traits.

Experimental Observations.

In studies performed during the earlier genomics program, 35S::G2467transformants were generally smaller than wild type, and formed ratherthin inflorescence stems that carried flowers that sometimes displayedabnormal, poorly developed organs. Additionally, rosette leaf senescenceappeared to occur prematurely.

Seedlings of overexpressing lines and wild-type controls were grown onlight deficient in red wavelengths (b/FR) and compared. Under theseconditions, the G2467 overexpressing lines did not exhibit a shadeavoidance phenotype. When individual lines were retested, one line didnot exhibit a shade avoidance phenotype whereas two lines were wild typein their response.

Utilities.

We have now analyzed 35S::G2467 seedlings grown under white light orwhite light deficient in wavelengths corresponding to the red region ofthe visible spectrum. 35S::G2467 seedlings did not exhibit a shadeavoidance phenotype under conditions where wild-type seedlings hadenhanced hypocotyl elongation.

The G2505 Clade of Transcription Factor Polypeptides G2505 (SEQ ID NO:817 and 818)

G2505 (AT4G10350) is a novel member of the NAC family of transcriptionfactors. G2505 and closely-related clade member sequences each comprisea conserved NAC domain that is expected to function in a similar mannerin each of these related sequences, that is, by playing a central rolein transcriptional regulation and in the conferring of shared traits.

Experimental Observations.

During our earlier genomics program, RT-PCR expression analysisindicated that G2505 was expressed at low or non-detectable levels inmost tissue types. However, higher levels of transcript were found inroots compared to other tissues. No induction of G2505 expression inleaf tissue was detected in response to environmental stress relatedconditions. At that time, it was extremely hard to obtain 35S::G2505transformants. A few lines were obtained and these were distinctly smalland dark in coloration. Only two of these lines produced sufficient seedfor physiology assays to be performed. However, both of those linesdisplayed enhanced performance in a severe drought assay.

G2505 overexpressing lines (from a mixed seed lot comprised of twoindependent transgenic lines) and wild-type controls were grown on lightdeficient in red wavelengths (b/FR) and compared. Under theseconditions, the G2505 overexpressing lines did not exhibit a shadeavoidance phenotype.

Utilities.

We have now analyzed 35S::G2505 lines grown under white light versuslight deficient in red light. 35S::G2505 seedlings exhibited a shadetolerant phenotype, suggesting that this gene might be involved in lightregulated development. However, it should be noted that as yet, thephenotype observed in a mixed batch of 35S::G2505 lines has not beenconfirmed by testing of individual lines. Nevertheless, this gene wasgiven an “A” ranking because the phenotype seen in the screen on mixedlines was moderately strong.

The G2550 Clade of Transcription Factor Polypeptides G2550 (SEQ ID NO:819 and 820)

We initially identified G2550 within sequence released by theArabidopsis Genome Initiative (GenBank accession AC023754) as a geneencoding a novel homeodomain protein of the BEL1 class. G2550 andclosely-related clade member sequences each comprise a conserved PDXdomain and a homeodomain domain that is expected to function in asimilar manner in each of these related sequences, that is, by playing acentral role in transcriptional regulation and in the conferring ofshared traits.

Experimental Observations.

During our genomics program, 35S::G2550 transgenic plants exhibited awild-type response to physiological assays, but displayed a number ofmorphological phenotypes. Initially, 35S::G2550 seedlings appeared wildtype at early stages. However, at the mid rosette stage, 35S::G2550lines were dark in coloration, displayed alterations in leaf shape, andformed shorter more compact inflorescences than controls. Following theswitch to flowering, 35S::G2550 transformants formed short, compact,bushy inflorescences, which had reduced internode elongation, andflowers bunched together at the tips. Fertility also appeared reduced,silique set was rather poor, and senescence was somewhat delayedcompared to wild type.

Seedlings of overexpressing lines and wild-type controls were grown onlight deficient in red wavelengths (b/FR) and compared. Under theseconditions, the G2550 overexpressing lines did not exhibit a shadeavoidance phenotype.

Utilities.

We have now analyzed 35S::G2550 seedlings grown under white light orwhite light deficient in wavelengths corresponding to the red region ofthe visible spectrum. 35S::G2550 seedlings did not exhibit a shadeavoidance phenotype under conditions where wild-type seedlings hadenhanced hypocotyl elongation. However, it be should noted that the35S::G2550 lines had short internodes and were short and compact atadult stages. Thus, the shade tolerance phenotype (reduced hypocotylelongation) observed in the current study could be part of the generaldwarf phenotype seen in these lines.

The G2640 Clade of Transcription Factor Polypeptides G2640 (SEQ ID NO:821 and 822)

G2640, a member of the SRS (SHORT INTERNODES, SHI) transcription factorfamily, corresponds to AT3G51060 as annotated by the Arabidopsis GenomeInitiative. The founding member of the SRS family has been implicated inthe suppression of GA induced cell elongation. G2640 and closely-relatedclade member sequences each comprise a conserved DUF702 domaincomprising at least one zinc finger domain that is expected to functionin a similar manner in each of these related sequences, that is, byplaying a central role in transcriptional regulation and in theconferring of shared traits.

Experimental Observations.

The function of G2640 was analyzed in our genomics program usingtransgenic plants in which a cDNA clone of the gene was expressed underthe control of the 35S promoter. While 35S::G2640 lines displayed awild-type response in all of the physiological assays, severaldevelopmental alterations were observed during morphological analysis.35S::G2640 transformants were smaller than wild type controls andproduced leaves with short petioles. Inflorescences from these plantswere compact and had very short internodes. Flowers displayed a varietyof non-specific abnormalities with organs often being poorly developed.As a result of such defects, the seed yield from most of the lines wasvery low.

Seedlings of overexpressing lines and wild-type controls were grown onlight deficient in red wavelengths (b/FR) and compared. Under theseconditions, the G2640 overexpressing lines did not exhibit a shadeavoidance phenotype. When individual lines were tested, two lines didnot exhibit a shade avoidance phenotype, and were observed to have longnarrow leaves.

Utilities.

We have now analyzed 35S::G2640 seedlings grown under white light orwhite light deficient in wavelengths corresponding to the red region ofthe visible spectrum. 35S::G2640 seedlings did not exhibit a shadeavoidance phenotype under conditions where wild-type seedlings hadenhanced hypocotyl elongation. This phenotype was only seen in two lines(an individual line repeat could not be performed using the third linebecause seed was not available).

It should be should noted that during our initial genomics program, weobserved that 35S::G2640 lines were rather short and compact at adultstages. Thus, the shade tolerance phenotype (reduced hypocotylelongation) observed in the current study could be part of the generalshort internode phenotype seen in these lines.

The G2686 Clade of Transcription Factor Polypeptides G2686 (SEQ ID NO:823 and 824)

G2686 corresponds to gene At1g66600, and it has also been described asWRKY63. G2686 and closely-related clade member sequences each comprise aconserved WRKY DNA-binding domain that is expected to function in asimilar manner in each of these related sequences, that is, by playing acentral role in transcriptional regulation and in the conferring ofshared traits.

Experimental Observations.

We had previously studied the function of the gene was using transgenicplants in which the gene was expressed under the control of the 35Spromoter. G2686 overexpressing lines behaved similarly to the wild-typecontrols in all physiological assays performed. However, inmorphological examinations, 35S::G2686 plants were observed to begenerally smaller than wild-type controls. Some lines also had shortrounded leaves.

Seedlings of overexpressing lines and wild-type controls were grown onlight deficient in red wavelengths (b/FR) and compared. Under theseconditions, the G2686 overexpressing lines did not exhibit a shadeavoidance phenotype. When individual lines were retested, two of threelines did not exhibit a shade avoidance phenotype.

Utilities.

We have now analyzed 35S::G2686 seedlings grown under white light orwhite light deficient in wavelengths corresponding to the red region ofthe visible spectrum. 35S::G2686 seedlings did not exhibit a shadeavoidance phenotype under conditions where wild-type seedlings hadenhanced hypocotyl elongation. However, the shade tolerance phenotype(reduced hypocotyl elongation) observed in the current study could bepart of the general small size phenotype that was earlier seen in theselines.

The G1073 Clade of Transcription Factor Polypeptides G2789 (SEQ ID NO:247 and 248)

The sequence of G2789 (AT3G60870) was obtained from the Arabidopsisgenome sequencing project (GenBank accession AL162295) based on itssequence similarity to other AT-hook related proteins. G2789 andclosely-related clade member sequences each comprise a conserved At-hookdomain and a second conserved domain (amino acids 68-208) or the DUF296domain (amino acids 86-201) that are expected to function in a similarmanner in each of these related sequences, that is, by playing a centralrole in transcriptional regulation and in the conferring of sharedtraits.

Experimental Observations.

During earlier studies, RT-PCR analysis indicated that G2789 wasexpressed at moderate levels in roots, flowers, embryos, siliques, andgerminating seeds. It was not detectable in rosette leaves or shoots. Nosignificant induction of G2789 was observed in rosette leaves by anycondition tested. At this time, the function of this gene was analyzedusing transgenic plants in which G2789 was expressed under the controlof the 35S promoter. Overexpression of G2789 in Arabidopsis resulted inseedlings that were ABA insensitive, had significantly more osmoticstress tolerance than wild-type plants, had altered carbon:nitrogenbalance sensing, were osmotic stress tolerant, and recovered better fromdrought that wild-type plants in soil-based drought assays.

Overexpression of G2789 also produced alterations in leaf and flowerdevelopment, and caused severe reductions in fertility.

Seedlings of overexpressing lines and wild-type controls were grown onlight deficient in red wavelengths (b/FR) and compared. Under theseconditions, the G2789 overexpressing lines did not exhibit a shadeavoidance phenotype. When the assay was repeated on individual lines,two of three lines analyzed showed a shade tolerant phenotype and hadshort hypocotyls compared with wild-type seedlings. One line was wildtype.

Utilities.

We have now analyzed 35S::G2789 lines grown under white light versuslight deficient in red light. Two of three lines tested exhibited ashade tolerance phenotype under conditions where wild-type seedlings hadenhanced hypocotyl elongation. Thus, G2789 might be involved in themodulation of light regulated development. It remains to be determinedwhether this function is related to the apparent involvement of the genein conferring abiotic stress tolerance and tolerance to low nutrientavailability.

Summary of Results for Above GIDs and Others Tested

TABLE 15 GIDs identified as conferring shade tolerance under low R:FRconditions PID of Shade Lines OEX tolerance Growth under Priority GIDGene family OE/KO tested construct phenotype¹ white light² Ranking³ G634TH OE 5, 6, 8 P1374 + − A G1048 bZIP OE 23, 24, 28 P1257 + − A G1100RING/C3H2C3 OE 27, 31, 38 P1353 ++ wt A G1412 NAC KO KO NA + wt A G1796AP2 OE 5, 28, 32 P2053 + − A G1995 Z-C2H2 OE 22, 37, 38 P2360 ++ wt AG2467 HS OE 7, 9, 10 P2744 + wt A G2505 NAC OE 86, 81 P2776 + wt A G2550HB OE 1, 3, 4 P16180 ++ wt A G2640 SRS OE 26, 30, 31 P2675 ++ + A G2686WRKY OE 5, 6, 10 P2095 + wt A G2789 AT-hook OE 5, 9, 19 P2058 + − A G24AP2 OE 2, 8, 11 P969 + wt B G38 AP2 OE 3, 6, 10 P179 + wt B G44 AP2 OE4, 5, 6 P182 + wt B G230 MYB-(R1)R2R3 OE 61, 63, 67 P810 + − B G234MYB-(R1)R2R3 OE 1, 2, 3 P201 + wt B G261 HS OE 1, 2, 3 P206 + + B G271AKR OE 3, 4, 5 P209 + − B G303 HLH/MYC OE 3, 8, 18 P1410 + wt B G359Z-C2H2 OE 4, 5, 7 P2379 + wt B G377 RING/C3H2C3 OE 7, 9, 20 P1354 + wt BG388 HB KO KO NA + − B G435 HB OE 4, 8, 16 P30 + − B G442 AP2 OE 6, 7, 8P909 + wt B G468 IAA OE 1, 22, 24 P2466 + wt B G571 bZIP OE 22, 26, 27P1557 + wt B G652 Z-CLDSH KO KO NA + − B G664 MYB-(R1)R2R3 OE 2, 3, 7P98 + − B G772 NAC OE 4, 15, 19 P868 + wt B G798 Z-Dof OE 1 P132 + wt BG818 HS OE 12, 16, 19 P1786 + wt B G971 AP2 OE 1, 14, 18 P1247 + wt BG974 AP2 OE 3, 4, 8 P1510 + wt B G988 SCR OE 21, 23, 25 P1475 + − BG1062 HLH/MYC KO KO NA + wt B G1069 AT-hook OE 41, 42, 64 P1178 + wt BG1129 HLH/MYC OE 2, 10, 16 P1298 + − B G1137 HLH/MYC OE 1, 14, 15 P938 +wt B G1425 NAC OE 22, 27, 28 P1361 + − B G1517 RING/C3HC4 OE 1, 2, 3P1096 + − B G1655 HLH/MYC OE 10, 14, 19 P1008 + − B G1743 RING/C3H2C3 OE1, 5, 7 P15028 + − B G1789 MYB-related OE 5, 11, 19 P1562 + wt B G1806bZIP OE 3, 6, 8 P1559 + wt B G1911 MYB-related OE 4, 5, 6 P989 + − BG2011 HS OE 5, 12, 18 P1813 + − B G2155 AT-hook OE 2, 8, 12 Pl742 + wt BG2215 bZIP-NIN OE 3, 5, 7 P1948 + wt B G2452 MYB-related OE 7, 11, 16P2023 + wt B G2455 YABBY OE 8, 11, 17 P2584 + wt B G2510 AP2 OE 12, 14,20 P2038 + wt B G2515 MADS OE 5, 41, 45 P13372 + wt B G2571 AP2 OE 1, 5,8 P1998 + wt B G2702 MYB-(R1)R2R3 OE 23, 29, 31 P13807 + wt B G2763HLH/MYC OE 1, 2, 5 P2387 + − B G2774 HLH/MYC OE 12, 15, 18 P16177 + wt BG2888 Z-C2H2 OE 21, 24, 27 P2656 + − B G2958 IAA OE 22, 26, 30 P15168 +wt B Table 15 Notes. All scores presented in Table 15 (other than wildtype) were based on data from two independent experiments on the seedbatches (assuming sufficient seed was available to repeat the experimenttwice). ¹Shade tolerance phenotype” column. Score of “++” indicates astrong suppression of shade responses; the phenotype was very consistentand growth was significantly above the normal levels of variabilityobserved for the assay. Score of “+” in the indicates a mild/moderatesuppression of shade responses; the response was consistent but was onlymoderately above the normal levels of variability observed for the assay²“Growth under white light” column. A score of “−” indicates that theseedlings from that line were generally smaller than wild-type controlsunder normal, white light conditions. A score of “+” indicates that theseedlings from that line were generally slightly larger than controlsunder normal conditions. A score of “wt” indicates that the seedlingswere normal under such conditions. ³GIDs which are considered top hitsand have been confirmed in multiple experiments are given an A ranking.GIDs that are considered potential leads but require confirmation infollow-up studies are given a B ranking. The “A” and “B” rankings arenot meant to be construed as an indication of the relative value andpotential utility of these candidate sequences, but represent the degreeof testing completeness.

Example XI: Identification of Homologous Sequences

This example describes identification of genes that are orthologous toArabidopsis thaliana transcription factors from a computer homologysearch.

Homologous sequences, including those of paralogs and orthologs fromArabidopsis and other plant species, were identified using databasesequence search tools, such as the Basic Local Alignment Search Tool(BLAST) (Altschul et al. (1990) supra; and Altschul et al. (1997)Nucleic Acid Res. 25: 3389-3402). The tblastx sequence analysis programswere employed using the BLOSUM-62 scoring matrix (Henikoff and Henikoff(1992) Proc. Natl. Acad. Sci. 89: 10915-10919). The entire NCBI GenBankdatabase was filtered for sequences from all plants except Arabidopsisthaliana by selecting all entries in the NCBI GenBank databaseassociated with NCBI taxonomic ID 33090 (Viridiplantae; all plants) andexcluding entries associated with taxonomic ID 3701 (Arabidopsisthaliana).

These sequences are compared to sequences representing genes of theinvention, for example, polynucleotides found in the Sequence Listing,using the Washington University TBLASTX algorithm (version 2.0a19MP) atthe default settings using gapped alignments with the filter “off”. Foreach polynucleotide sequence found in the Sequence Listing, individualcomparisons were ordered by probability score (P-value), where the scorereflects the probability that a particular alignment occurred by chance.For example, a score of 3.6E-40 is 3.6×10-40. In addition to P-values,comparisons were also scored by percentage identity. Percentage identityreflects the degree to which two segments of DNA or protein areidentical over a particular length. Examples of sequences so identifiedare presented in Tables 8 and 9. The percent sequence identity amongthese sequences can be as low as 47%, or even lower sequence identity.

Candidate paralogous sequences were identified among Arabidopsistranscription factors through alignment, identity, and phylogenicrelationships. Candidate orthologous sequences were identified fromproprietary unigene sets of plant gene sequences in Zea mays, Glycinemax and Oryza sativa based on significant homology to Arabidopsistranscription factors. These candidates were reciprocally compared tothe set of Arabidopsis transcription factors. If the candidate showedmaximal similarity in the protein domain to the eliciting transcriptionfactor or to a paralog of the eliciting transcription factor, then itwas considered to be an ortholog. Identified non-Arabidopsis sequencesthat were shown in this manner to be orthologous to the Arabidopsissequences are provided in Tables 8 and 9.

Example XII: Screen of Plant cDNA Library for Sequence Encoding aTranscription Factor DNA Binding Domain that Binds to a TranscriptionFactor Binding Promoter Element and Demonstration of ProteinTranscription Regulation Activity

The “one-hybrid” strategy (Li and Herskowitz (1993) Science 262:1870-1874) is used to screen for plant cDNA clones encoding apolypeptide comprising a transcription factor DNA binding domain, aconserved domain. In brief, yeast strains are constructed that contain alacZ reporter gene with either wild-type or mutant transcription factorbinding promoter element sequences in place of the normal UAS (upstreamactivator sequence) of the GAL4 promoter. Yeast reporter strains areconstructed that carry transcription factor binding promoter elementsequences as UAS elements are operably linked upstream (5′) of a lacZreporter gene with a minimal GAL4 promoter. The strains are transformedwith a plant expression library that contains random cDNA inserts fusedto the GAL4 activation domain (GAL4-ACT) and screened for blue colonyformation on X-gal-treated filters (X-gal:5-bromo-4-chloro-3-indolyl-ß-D-galactoside; Invitrogen Corporation,Carlsbad Calif.). Alternatively, the strains are transformed with a cDNApolynucleotide encoding a known transcription factor DNA binding domainpolypeptide sequence.

Yeast strains carrying these reporter constructs produce low levels ofβ-galactosidase and form white colonies on filters containing X-gal. Thereporter strains carrying wild-type transcription factor bindingpromoter element sequences are transformed with a polynucleotide thatencodes a polypeptide comprising a plant transcription factor DNAbinding domain operably linked to the acidic activator domain of theyeast GAL4 transcription factor, “GAL4-ACT”. The clones that contain apolynucleotide encoding a transcription factor DNA binding domainoperably linked to GAL4-ACT can bind upstream of the lacZ reporter genescarrying the wild-type transcription factor binding promoter elementsequence, activate transcription of the lacZ gene and result in yeastforming blue colonies on X-gal-treated filters.

Upon screening about 2×10⁶ yeast transformants, positive cDNA clones areisolated; i.e., clones that cause yeast strains carrying lacZ reportersoperably linked to wild-type transcription factor binding promoterelements to form blue colonies on X-gal-treated filters. The cDNA clonesdo not cause a yeast strain carrying a mutant type transcription factorbinding promoter elements fused to LacZ to turn blue. Thus, apolynucleotide encoding transcription factor DNA binding domain, aconserved domain, is shown to activate transcription of a gene.

Example XIII: Gel Shift Assays

The presence of a transcription factor comprising a DNA binding domainwhich binds to a DNA transcription factor binding element is evaluatedusing the following gel shift assay. The transcription factor isrecombinantly expressed and isolated from E. coli or isolated from plantmaterial. Total soluble protein, including transcription factor, (40 ng)is incubated at room temperature in 10 μl of 1× binding buffer (15 mMHEPES (pH 7.9), 1 mM EDTA, 30 mM KCl, 5% glycerol, 5% bovine serumalbumin, 1 mM DTT) plus 50 ng poly(dl-dC):poly(dl-dC) (Pharmacia,Piscataway N.J.) with or without 100 ng competitor DNA. After 10 minutesincubation, probe DNA comprising a DNA transcription factor bindingelement (1 ng) that has been ³²P-labeled by end-filling (Sambrook et al.supra) is added and the mixture incubated for an additional 10 minutes.Samples are loaded onto polyacrylamide gels (4% w/v) and fractionated byelectrophoresis at 150V for 2h (Sambrook et al. supra). The degree oftranscription factor-probe DNA binding is visualized usingautoradiography. Probes and competitor DNAs are prepared fromoligonucleotide inserts ligated into the BamHI site of pUC118 (Vieira etal. (1987) Methods Enzymol. 153: 3-11). Orientation and concatenationnumber of the inserts are determined by dideoxy DNA sequence analysis(Sambrook et al. supra). Inserts are recovered after restrictiondigestion with EcoRI and HindIII and fractionation on polyacrylamidegels (12% w/v) (Sambrook et al. supra).

Example XIV. Transformation of Dicots

Crop species overexpressing members of the G1792 clade of transcriptionfactor polypeptides have been shown experimentally to produce plantswith increased tolerance to disease. This observation indicates thatthese genes, when overexpressed, will result in larger yields of variousplant species, particularly during conditions of biotic stress.

Thus, transcription factor sequences listed in the Sequence Listingrecombined into pMEN20 or pMEN65 expression vectors may be transformedinto a plant for the purpose of modifying plant traits. The cloningvector may be introduced into a variety of cereal plants by means wellknown in the art such as, for example, direct DNA transfer orAgrobacterium tumefaciens-mediated transformation. It is now routine toproduce transgenic plants using most dicot plants (see Weissbach andWeissbach, (1989) supra; Gelvin et al. (1990) supra; Herrera-Estrella etal. (1983) supra; Bevan (1984) supra; and Klee (1985) supra). Methodsfor analysis of traits are routine in the art and examples are disclosedabove.

Methods for transforming cotton may be found in U.S. Pat. Nos.5,004,863, 5,159,135 and 5,518,908; for transforming Brassica speciesmay be found in U.S. Pat. No. 5,463,174; for transforming peanut plantsmay be found in Cheng et al. (1996) Plant Cell Rep. 15: 653-657, andMcKently et al. (1995) Plant Cell Rep. 14: 699-703; and for transformingpea may be found in Grant et al. (1995) Plant Cell Rep. 15: 254-258.

Numerous protocols for the transformation of tomato and soy plants havebeen previously described, and are well known in the art. Gruber et al.((1993) in Methods in Plant Molecular Biology and Biotechnology, p.89-119, Glick and Thompson, eds., CRC Press, Inc., Boca Raton) describeseveral expression vectors and culture methods that may be used for cellor tissue transformation and subsequent regeneration. For soybeantransformation, methods are described by Mild et al. (1993) in Methodsin Plant Molecular Biology and Biotechnology, p. 67-88, Glick andThompson, eds., CRC Press, Inc., Boca Raton; and U.S. Pat. No.5,563,055, (Townsend and Thomas), issued Oct. 8, 1996.

There are a substantial number of alternatives to Agrobacterium-mediatedtransformation protocols, other methods for the purpose of transferringexogenous genes into soybeans or tomatoes. One such method ismicroprojectile-mediated transformation, in which DNA on the surface ofmicroprojectile particles is driven into plant tissues with a biolisticdevice (see, for example, Sanford et al., (1987) Part. Sci. Technol.5:27-37; Christou et al. (1992) Plant. J. 2: 275-281; Sanford (1993)Methods Enzymol. 217: 483-509; Klein et al. (1987) Nature 327: 70-73;U.S. Pat. No. 5,015,580 (Christou et al), issued May 14, 1991; and U.S.Pat. No. 5,322,783 (Tomes et al.), issued Jun. 21, 1994.

Alternatively, sonication methods (see, for example, Zhang et al. (1991)Bio/Technology 9: 996-997); direct uptake of DNA into protoplasts usingCaCl2 precipitation, polyvinyl alcohol or poly-L-ornithine (see, forexample, Hain et al. (1985) Mol. Gen. Genet. 199: 161-168; Draper etal., Plant Cell Physiol. 23: 451-458 (1982)); liposome or spheroplastfusion (see, for example, Deshayes et al. (1985) EMBO J., 4: 2731-2737;Christou et al. (1987) Proc. Natl. Acad. Sci. USA 84: 3962-3966); andelectroporation of protoplasts and whole cells and tissues (see, forexample, Donn et al. (1990) in Abstracts of VIIth International Congresson Plant Cell and Tissue Culture IAPTC, A2-38: 53; D'Halluin et al.(1992) Plant Cell 4: 1495-1505; and Spencer et al. (1994) Plant Mol.Biol. 24: 51-61) have been used to introduce foreign DNA and expressionvectors into plants.

After a plant or plant cell is transformed (and the latter regeneratedinto a plant), the transformed plant may be crossed with itself or aplant from the same line, a non-transformed or wild-type plant, oranother transformed plant from a different transgenic line of plants.Crossing provides the advantages of producing new and often stabletransgenic varieties. Genes and the traits they confer that have beenintroduced into a tomato or soybean line may be moved into distinct lineof plants using traditional backcrossing techniques well known in theart. Transformation of tomato plants may be conducted using theprotocols of Koornneef et al (1986) In Tomato Biotechnology: Alan R.Liss, Inc., 169-178, and in U.S. Pat. No. 6,613,962, the latter methoddescribed in brief here. Eight day old cotyledon explants areprecultured for 24 hours in Petri dishes containing a feeder layer ofPetunia hybrida suspension cells plated on MS medium with 2% (w/v)sucrose and 0.8% agar supplemented with 10 μM α-naphthalene acetic acidand 4.4 μM 6-benzylaminopurine. The explants are then infected with adiluted overnight culture of Agrobacterium tumefaciens containing anexpression vector comprising a polynucleotide of the invention for 5-10minutes, blotted dry on sterile filter paper and cocultured for 48 hourson the original feeder layer plates. Culture conditions are as describedabove. Overnight cultures of Agrobacterium tumefaciens are diluted inliquid MS medium with 2% (w/v/) sucrose, pH 5.7) to an OD₆₀₀ of 0.8.

Following cocultivation, the cotyledon explants are transferred to Petridishes with selective medium comprising MS medium with 4.56 μM zeatin,67.3 μM vancomycin, 418.9 μM cefotaxime and 171.6 μM kanamycin sulfate,and cultured under the culture conditions described above. The explantsare subcultured every three weeks onto fresh medium. Emerging shoots aredissected from the underlying callus and transferred to glass jars withselective medium without zeatin to form roots. The formation of roots ina kanamycin sulfate-containing medium is a positive indication of asuccessful transformation.

Transformation of soybean plants may be conducted using the methodsfound in, for example, U.S. Pat. No. 5,563,055. In this method, soybeanseed is surface sterilized by exposure to chlorine gas evolved in aglass bell jar. Seeds are germinated by plating on 1/10 strength agarsolidified medium without plant growth regulators and culturing at 28°C. with a 16 hour day length. After three or four days, seed may beprepared for cocultivation. The seedcoat is removed and the elongatingradicle removed 3-4 mm below the cotyledons.

Overnight cultures of Agrobacterium tumefaciens harboring the expressionvector comprising a polynucleotide of the invention are grown to logphase, pooled, and concentrated by centrifugation. Inoculations areconducted in batches such that each plate of seed was treated with anewly resuspended pellet of Agrobacterium. The pellets are resuspendedin 20 ml inoculation medium. The inoculum is poured into a Petri dishcontaining prepared seed and the cotyledonary nodes are macerated with asurgical blade. After 30 minutes the explants are transferred to platesof the same medium that has been solidified. Explants are embedded withthe adaxial side up and level with the surface of the medium andcultured at 22° C. for three days under white fluorescent light. Theseplants may then be regenerated according to methods well established inthe art, such as by moving the explants after three days to a liquidcounter-selection medium (see U.S. Pat. No. 5,563,055).

The explants may then be picked, embedded and cultured in solidifiedselection medium. After one month on selective media transformed tissuebecomes visible as green sectors of regenerating tissue against abackground of bleached, less healthy tissue. Explants with green sectorsare transferred to an elongation medium. Culture is continued on thismedium with transfers to fresh plates every two weeks. When shoots are0.5 cm in length they may be excised at the base and placed in a rootingmedium.

Example XV: Altered C/N Sensing and Increased Shade and Abiotic StressTolerance in Monocots

Cereal plants such as, but not limited to, corn, wheat, rice, sorghum,or barley, may be transformed with the present polynucleotide sequences,including monocot or dicot-derived sequences such as those presented inTables 1, 3, 8 or 9, cloned into a vector such as pGA643 and containinga kanamycin-resistance marker, and expressed constitutively under, forexample, the CaMV 35S or COR15 promoters. pMEN20 or pMEN65 and otherexpression vectors may also be used for the purpose of modifying planttraits. For example, pMEN020 may be modified to replace the NptII codingregion with the BAR gene of Streptomyces hygroscopicus that confersresistance to phosphinothricin. The KpnI and BglII sites of the Bar geneare removed by site-directed mutagenesis with silent codon changes.

The cloning vector may be introduced into a variety of cereal plants bymeans well known in the art including direct DNA transfer orAgrobacterium tumefaciens-mediated transformation. The latter approachmay be accomplished by a variety of means, including, for example, thatof U.S. Pat. No. 5,591,616, in which monocotyledon callus is transformedby contacting dedifferentiating tissue with the Agrobacterium containingthe cloning vector.

The sample tissues are immersed in a suspension of 3×10⁻⁹ cells ofAgrobacterium containing the cloning vector for 3-10 minutes. The callusmaterial is cultured on solid medium at 25° C. in the dark for severaldays. The calli grown on this medium are transferred to Regenerationmedium. Transfers are continued every 2-3 weeks (2 or 3 times) untilshoots develop. Shoots are then transferred to Shoot-Elongation mediumevery 2-3 weeks. Healthy looking shoots are transferred to rootingmedium and after roots have developed, the plants are placed into moistpotting soil.

The transformed plants are then analyzed for the presence of the NPTIIgene/kanamycin resistance by ELISA, using the ELISA NPTII kit from5Prime-3Prime Inc. (Boulder, Colo.).

It is also routine to use other methods to produce transgenic plants ofmost cereal crops (Vasil (1994) Plant Mol. Biol. 25: 925-937) such ascorn, wheat, rice, sorghum (Cassas et al. (1993) Proc. Natl. Acad. Sci.USA 90: 11212-11216, and barley (Wan and Lemeaux (1994) Plant Physiol.104:37-48). DNA transfer methods such as the microprojectile method canbe used for corn (Fromm et al. (1990) Bio/Technol. 8: 833-839);Gordon-Kamm et al. (1990) Plant Cell 2: 603-618; Ishida (1990) NatureBiotechnol. 14:745-750), wheat (Vasil et al. (1992) Bio/Technol.10:667-674; Vasil et al. (1993) Bio/Technol. 11:1553-1558; Weeks et al.(1993) Plant Physiol. 102:1077-1084), and rice (Christou (1991)Bio/Technol. 9:957-962; Hiei et al. (1994) Plant J. 6:271-282; Aldemitaand Hodges (1996) Planta 199:612-617; and Hiei et al. (1997) Plant Mol.Biol. 35:205-218). For most cereal plants, embryogenic cells derivedfrom immature scutellum tissues are the preferred cellular targets fortransformation (Hiei et al. (1997) Plant Mol. Biol. 35:205-218; Vasil(1994) Plant Mol. Biol. 25: 925-937). For transforming corn embryogeniccells derived from immature scutellar tissue using microprojectilebombardment, the A188XB73 genotype is the preferred genotype (Fromm etal. (1990) Bio/Technol. 8: 833-839; Gordon-Kamm et al. (1990) Plant Cell2: 603-618). After microprojectile bombardment the tissues are selectedon phosphinothricin to identify the transgenic embryogenic cells(Gordon-Kamm et al. (1990) Plant Cell 2: 603-618). Transgenic plants areregenerated by standard corn regeneration techniques (Fromm et al.(1990) Bio/Technol. 8: 833-839; Gordon-Kamm et al. (1990) Plant Cell 2:603-618).

Northern blot analysis, RT-PCR or microarray analysis of theregenerated, transformed plants may be used to show expression of G1792and related genes that are capable of conferring tolerance to biotic orabiotic stress.

To verify the ability to confer abiotic stress tolerance, mature plantsoverexpressing a transcription factor of the invention, oralternatively, seedling progeny of these plants, may be challenged in anabiotic stress assay, such as a drought, heat, high salt, or freezingassay, in an osmotic stress condition that may also measure alteredsugar sensing, such as a high sugar condition, in a shade toleranceassay, or in a C/N sensing assay to identify plants with altered stressor shade tolerance of altered C/N sensing. By comparing wild type andtransgenic plants similarly treated, the transgenic plants may be shownto have greater tolerance to abiotic stress.

After a monocot plant or plant cell has been transformed (and the latterregenerated into a plant) and shown to have greater tolerance to bioticor abiotic stress, or produce greater yield relative to a control plantunder the stress conditions, the transformed monocot plant may becrossed with itself or a plant from the same line, a non-transformed orwild-type monocot plant, or another transformed monocot plant from adifferent transgenic line of plants.

Example XVI: Genes that Confer Significant Improvements toNon-Arabidopsis Species

The function of specific orthologs of transcription factors of theinvention has been analyzed and may be further characterized byincorporation into crop plants. The function of specific orthologs ofthe sequences in the Sequence Listing may be analyzed through theiraltered expression (e.g., ectopic overexpression, or knocking out) inplants, using constitutive, inducible, or tissue specific regulatoryelements, as disclosed above. These sequences include polynucleotidesequences found in the Sequence Listing such as, for example:

(i) those sequences conferring drought tolerance found in Arabidopsisthaliana SEQ ID NO: 2 (G47) and SEQ ID NO: 12 (G2133); Oryza sativa(japonica cultivar-group) SEQ ID NO: 98 (G3649), SEQ ID NO: 100 (G3651),and SEQ ID NO: 90 (G3644); Glycine max SEQ ID NO: 88 (G3643); Zinniaelegans SEQ ID NO: 96 (G3647); Brassica rapa subsp. Pekinensis SEQ IDNO: 92 (G3645); and Brassica oleracea SEQ ID NO: 94 (G3646);

(ii) those sequences conferring altered C/N sensing found in Arabidopsisthaliana SEQ ID NO: 234, 286, 312, and 32 (G682, G226, G1816, and G2718;Oryza sativa SEQ ID NO: 326 and 328 (G3392 and G3393); Glycine max SEQID NO: 372, 374, 376, 378, 380, and 382 (G3445, G3446, G3447, G3448,G3449, and G3450); and Zea mays SEQ ID NO: 360 and 370 (G3431 andG3444); and

(iii) those sequences conferring shade tolerance found in Arabidopsisthaliana SEQ ID NO: 232 (G634), SEQ ID NO: 818 (G2505), and SEQ ID NO:248 (G2789), and G2789 orthologs in Glycine max (Gma_54935598) and Pinustaeda (Pta_515799222, Pta_516786360, Pta_516788492, and Pta_516802054).

The polynucleotide and polypeptide sequences derived from monocots maybe used to transform both monocot and dicot plants, and those derivedfrom dicots may be used to transform either group, although some ofthese sequences will function best if the gene is transformed into aplant from the same group as that from which the sequence is derived.

Transformation procedures are provided in these Examples, and may employthe use of an expression vector. After the vector is introduced into aplant cell, a plant may be regenerated from the cell, after which theplant is allowed to overexpress one of the polypeptides of the inventionthat have the property of increasing abiotic stress tolerance, shadetolerance, or altered C/N sensing in the transgenic plant. Plants withthese altered traits may be identified by comparison with wild-type ornon-transformed plants that do not overexpress the polypeptide, afterwhich one or more plant with a desirable degree of one or more improvedtraits may be selected. In this manner, plants with enhanced shadetolerance, increased abiotic stress tolerance, altered C/N sensing, ormore than one of these altered traits may be selected.

For drought tolerance-related analysis, seeds of these transgenic plantsare subjected to germination assays to measure sucrose sensing. Sterilemonocot seeds, including, but not limited to, corn, rice, wheat, rye andsorghum, as well as dicots including, but not limited to soybean andalfalfa, are sown on 80% MS medium plus vitamins with 9.4% sucrose;control media lack sucrose. All assay plates are then incubated at 22°C. under 24-hour light, 120-130 μEin/m²/s, in a growth chamber.Evaluation of germination and seedling vigor is then conducted threedays after planting. Overexpressors of these sequences may be found tobe more tolerant to high sucrose by having better germination, longerradicles, and more cotyledon expansion. These results would indicatethat overexpressors of the orthologs in the Sequence Listing areinvolved in sucrose-specific sugar sensing.

Plants overexpressing these orthologs may also be subjected tosoil-based drought assays to identify those lines that are more tolerantto water deprivation than wild-type control plants. Generally, orthologoverexpressing plants will appear significantly larger and greener, withless wilting or desiccation, than wild-type controls plants,particularly after a period of water deprivation is followed byrewatering and a subsequent incubation period.

For C/N sensing-related analysis, seeds of these transgenic plants aresubjected to germination or growth assays to measure C/N sensing ortolerance to low nitrogen. Sterilized monocot seeds, including, but notlimited to, corn, rice, wheat, rye and sorghum, as well as dicotsincluding, but not limited to soybean and alfalfa, are sown on basalmedia comprising 80% MS+Vitamins.

The sterile seeds sown onto plates containing media based on 80% MSwithout a nitrogen source. For C/N assays, the media contains 3%sucrose. The −N/+Gln media the same media, supplemented with 1 mMglutamine, is used. Plates are incubated in a 24-hour light C (120-130μEins⁻² m⁻¹) growth chamber at 22° C. Evaluation of germination andseedling vigor is performed five days after planting. Overexpressors ofthese genes that are more tolerant to low nitrogen than control plantshave better germination, longer radicles, more cotyledon expansion, moreroot hairs, greater root mass, more vegetative growth, a greenerappearance, or less anthocyanin. The latter (production of lessanthocyanin on these media) is generally associated with increasedtolerance to nitrogen limitation.

A transgene responsible for the altered response is likely involved inthe plant's ability to perceive their carbon and nitrogen status.

For shade tolerance-related analysis, seeds of these transgenic plantsare subjected to germination or growth assays to measure shadetolerance. Sterilized monocot seeds, including, but not limited to,corn, rice, wheat, rye and sorghum, as well as dicots including, but notlimited to soybean and alfalfa, are sown on 80% MS medium plus vitamins.Plates are incubated at 22° C. under 24-hour light (about 50μEinsteins⁻² m⁻¹) under both white light (control) and under lightdepleted in red wavelengths. Seedlings are then assessed for shadetolerance at 7 days, and shade tolerance is scored by visually observingdifferences in hypocotyl length compared with control seedlings grownunder white light and grown under light lacking the red wavelengths.

Overexpressors of these sequences may be found to be more tolerant tolow light by having altered morphological characteristics associatedwith a shade tolerant phenotype, or improved growth or yield inconditions of low light. Overexpressors of these genes may also be foundto be more tolerant to shade or abiotic stresses, and may show alteredcotyledon, altered hypocotyl, altered leaf orientation, altered petiole,and/or constitutive photomorphogenesis, better germination, longerradicles, more cotyledon expansion, more vegetative growth, a greenerappearance, or less anthocyanin in stress conditions. These resultswould indicate that overexpressors of the orthologs in the SequenceListing are involved in shade tolerance responses.

Plants overexpressing these orthologs may also be subjected to low lightor abiotic stress assays to identify those lines that are more tolerantto low light conditions or abiotic stresses than wild-type controlplants in these conditions. Generally, ortholog overexpressing plantswill show morphological features that are associated with a shadeavoidance phenotype (e.g., altered cotyledon, altered hypocotyl, alteredleaf orientation, altered petiole, and/or constitutivephotomorphogenesis), and may also appear larger, greener, and healthierthan wild-type controls plants.

Example XVII: Identification of Orthologous and Paralogous Sequences

Orthologs to Arabidopsis genes may identified by several methods,including hybridization, amplification, or bioinformatically. Thisexample describes how one may identify homologs to the Arabidopsis AP2family transcription factor CBF1, which confers tolerance to abioticstresses (Thomashow et al. (2002) U.S. Pat. No. 6,417,428), and anexample to confirm the function of homologous sequences. In thisexample, orthologs to CBF1 were found in canola (Brassica napus) usingpolymerase chain reaction (PCR).

Degenerate primers were designed for regions of AP2 binding domain andoutside of the AP2 (carboxyl terminal domain; U.S. Pat. No. 6,417,428):

Mol 368 (reverse) (SEQ ID NO: 1437) 5′-CAY CCN ATH TAY MGN GGN GT-3′Mol 378 (forward) (SEQ ID NO: 1438) 5′-GGN ARN ARC ATN CCY TCN GCC-3′(Y: C/T, N: A/C/G/T, H: A/C/T, M: A/C, R: A/G)

Primer Mol 368 is in the AP2 binding domain of CBF1 (amino acidsequence: His-Pro-Ile-Tyr-Arg-Gly-Val; SEQ ID NO: 1439) while primer Mol378 is outside the AP2 domain (carboxyl terminal domain) (amino acidsequence: Met-Ala-Glu-Gly-Met-Leu-Leu-Pro); SEQ ID NO: 1440).

The genomic DNA isolated from B. napus was PCR-amplified by using theseprimers following these conditions: an initial denaturation step of 2min at 93° C.; 35 cycles of 93° C. for 1 min, 55° C. for 1 min, and 72°C. for 1 min; and a final incubation of 7 min at 72° C. at the end ofcycling.

The PCR products were separated by electrophoresis on a 1.2% agarose geland transferred to nylon membrane and hybridized with the AT CBF1 probeprepared from Arabidopsis genomic DNA by PCR amplification. Thehybridized products were visualized by colorimetric detection system(Boehringer Mannheim) and the corresponding bands from a similar agarosegel were isolated using the Qiagen Extraction Kit (Qiagen). The DNAfragments were ligated into the TA clone vector from TOPO TA Cloning Kit(Invitrogen) and transformed into E. coli strain TOP10 (Invitrogen).

Seven colonies were picked and the inserts were sequenced on an ABI 377machine from both strands of sense and antisense after plasmid DNAisolation. The DNA sequence was edited by sequencer and aligned with theAtCBF1 by GCG software and NCBI blast searching.

The nucleic acid sequence and amino acid sequence of one canola orthologfound in this manner (bnCBF1; U.S. Pat. No. 6,417,428) identified bythis process is shown in the Sequence Listing.

The aligned amino acid sequences show that the bnCBF1 gene has 88%identity with the Arabidopsis sequence in the AP2 domain region and 85%identity with the Arabidopsis sequence outside the AP2 domain whenaligned for two insertion sequences that are outside the AP2 domain.

Similarly, paralogous sequences to Arabidopsis genes, such as CBF1, mayalso be identified.

Two paralogs of CBF1 from Arabidopsis thaliana: CBF2 and CBF3. CBF2 andCBF3 have been cloned and sequenced as described below. The sequences ofthe DNA and encoded proteins are set forth in U.S. Pat. No. 6,417,428.

A lambda cDNA library prepared from RNA isolated from Arabidopsisthaliana ecotype Columbia (Lin and Thomashow (1992) Plant Physiol. 99:519-525) was screened for recombinant clones that carried insertsrelated to the CBF1 gene (Stockinger et al. (1997) Proc. Natl. Acad.Sci. 94:1035-1040). CBF1 was ³²P-radiolabeled by random priming(Sambrook et al. supra) and used to screen the library by theplaque-lift technique using standard stringent hybridization and washconditions (Hajela et al. (1990) Plant Physiol. 93:1246-1252; Sambrooket al. supra) 6×SSPE buffer, 60° C. for hybridization and 0.1×SSPEbuffer and 60° C. for washes). Twelve positively hybridizing clones wereobtained and the DNA sequences of the cDNA inserts were determined. Theresults indicated that the clones fell into three classes. One classcarried inserts corresponding to CBF1. The two other classes carriedsequences corresponding to two different homologs of CBF1, designatedCBF2 and CBF3. The nucleic acid sequences and predicted protein codingsequences for Arabidopsis CBF1, CBF2, CBF3, and the Brassica napus CBFortholog are set forth in U.S. Pat. No. 6,417,428.

A comparison of the nucleic acid sequences of Arabidopsis CBF1, CBF2 andCBF3 indicate that they are 83 to 85% identical as shown in Table 16.

TABLE 16 Percent identity^(a) DNA^(b) Polypeptide cbf1/cbf2 85 86cbf1/cbf3 83 84 cbf2/cbf3 84 85 ^(a)Percent identity was determinedusing the Clustal algorithm from the MEGALIGN program (DNASTAR, Inc.).^(b)Comparisons of the nucleic acid sequences of the open reading framesare shown.

Similarly, the amino acid sequences of the three CBF polypeptides rangefrom 84 to 86% identity. An alignment of the three amino acid sequencesreveals that most of the differences in amino acid sequence occur in theacidic C-terminal half of the polypeptide. This region of CBF1 serves asan activation domain in both yeast and Arabidopsis (not shown).

Residues 47 to 106 of CBF1 correspond to the AP2 domain of the protein,a DNA binding motif that to date, has only been found in plant proteins.A comparison of the AP2 domains of CBF1, CBF2 and CBF3 indicates thatthere are a few differences in amino acid sequence. These differences inamino acid sequence might have an effect on DNA binding specificity.

Example XVIII: Transformation of Canola with a Plasmid Containing CBF1,CBF2, or CBF3

After identifying homologous genes to CBF1, canola was transformed witha plasmid containing the Arabidopsis CBF1, CBF2, or CBF3 genes clonedinto the vector pGA643 (An (1987) Methods Enzymol. 253: 292). In theseconstructs the CBF genes were expressed constitutively under the CaMV35S promoter. In addition, the CBF1 gene was cloned under the control ofthe Arabidopsis COR15 promoter in the same vector pGA643. Each constructwas transformed into Agrobacterium strain GV3101. TransformedAgrobacteria were grown for 2 days in minimal AB medium containingappropriate antibiotics.

Spring canola (B. napus cv. Westar) was transformed using the protocolof Moloney et al. ((1989) Plant Cell Reports 8: 238) with somemodifications as described. Briefly, seeds were sterilized and plated onhalf strength MS medium, containing 1% sucrose. Plates were incubated at24° C. under 60-80 μE/m²s light using a 16 hour light/8 hour darkphotoperiod. Cotyledons from 4-5 day old seedlings were collected, thepetioles cut and dipped into the Agrobacterium solution. The dippedcotyledons were placed on co-cultivation medium at a density of 20cotyledons/plate and incubated as described above for 3 days. Explantswere transferred to the same media, but containing 300 mg/l timentin(SmithKline Beecham, Pa.) and thinned to 10 cotyledons/plate. After 7days explants were transferred to Selection/Regeneration medium.Transfers were continued every 2-3 weeks (2 or 3 times) until shoots haddeveloped. Shoots were transferred to Shoot-Elongation medium every 2-3weeks. Healthy looking shoots were transferred to rooting medium. Oncegood roots had developed, the plants were placed into moist pottingsoil.

The transformed plants were then analyzed for the presence of the NPTIIgene/kanamycin resistance by ELISA, using the ELISA NPTII kit from5Prime-3Prime Inc. (Boulder, Colo.). Approximately 70% of the screenedplants were NPTII positive. Only those plants were further analyzed.

From Northern blot analysis of the plants that were transformed with theconstitutively expressing constructs, showed expression of the CBF genesand all CBF genes were capable of inducing the Brassica napuscold-regulated gene BN115 (homolog of the Arabidopsis COR15 gene). Mostof the transgenic plants appear to exhibit a normal growth phenotype. Asexpected, the transgenic plants are more freezing tolerant than thewild-type plants. Using the electrolyte leakage of leaves test, thecontrol showed a 50% leakage at −2 to −3° C. Spring canola transformedwith either CBF1 or CBF2 showed a 50% leakage at −6 to −7° C. Springcanola transformed with CBF3 shows a 50% leakage at about −10 to −15° C.Winter canola transformed with CBF3 may show a 50% leakage at about −16to −20° C. Furthermore, if the spring or winter canola are coldacclimated the transformed plants may exhibit a further increase infreezing tolerance of at least −2° C.

To test salinity tolerance of the transformed plants, plants werewatered with 150 mM NaCl. Plants overexpressing CBF1, CBF2 or CBF3 grewbetter compared with plants that had not been transformed with CBF1,CBF2 or CBF3.

These results demonstrate that homologs of Arabidopsis transcriptionfactors can be identified and shown to confer similar functions innon-Arabidopsis plant species.

Example IXX: Cloning of Transcription Factor Promoters

Promoters are isolated from transcription factor genes that have geneexpression patterns useful for a range of applications, as determined bymethods well known in the art (including transcript profile analysiswith cDNA or oligonucleotide microarrays, Northern blot analysis,semi-quantitative or quantitative RT-PCR). Interesting gene expressionprofiles are revealed by determining transcript abundance for a selectedtranscription factor gene after exposure of plants to a range ofdifferent experimental conditions, and in a range of different tissue ororgan types, or developmental stages. Experimental conditions to whichplants are exposed for this purpose includes cold, heat, drought,osmotic challenge, varied hormone concentrations (ABA, GA, auxin,cytokinin, salicylic acid, brassinosteroid), pathogen and pestchallenge. The tissue types and developmental stages include stem, root,flower, rosette leaves, cauline leaves, siliques, germinating seed, andmeristematic tissue. The set of expression levels provides a patternthat is determined by the regulatory elements of the gene promoter.

Transcription factor promoters for the genes disclosed herein areobtained by cloning 1.5 kb to 2.0 kb of genomic sequence immediatelyupstream of the translation start codon for the coding sequence of theencoded transcription factor protein. This region includes the 5′-UTR ofthe transcription factor gene, which can comprise regulatory elements.The 1.5 kb to 2.0 kb region is cloned through PCR methods, using primersthat include one in the 3′ direction located at the translation startcodon (including appropriate adaptor sequence), and one in the 5′direction located from 1.5 kb to 2.0 kb upstream of the translationstart codon (including appropriate adaptor sequence). The desiredfragments are PCR-amplified from Arabidopsis Col-0 genomic DNA usinghigh-fidelity Taq DNA polymerase to minimize the incorporation of pointmutation(s). The cloning primers incorporate two rare restriction sites,such as NotI and Sfi1, found at low frequency throughout the Arabidopsisgenome. Additional restriction sites are used in the instances where aNotI or Sfi1 restriction site is present within the promoter.

The 1.5-2.0 kb fragment upstream from the translation start codon,including the 5′-untranslated region of the transcription factor, iscloned in a binary transformation vector immediately upstream of asuitable reporter gene, or a transactivator gene that is capable ofprogramming expression of a reporter gene in a second gene construct.Reporter genes used include green fluorescent protein (and relatedfluorescent protein color variants), β-glucuronidase, and luciferase.Suitable transactivator genes include LexA-GAL4, along with atransactivatable reporter in a second binary plasmid (as disclosed inU.S. patent application Ser. No. 09/958,131, incorporated herein byreference). The binary plasmid(s) is transferred into Agrobacterium andthe structure of the plasmid confirmed by PCR. These strains areintroduced into Arabidopsis plants as described in other examples, andgene expression patterns determined according to standard methods knowto one skilled in the art for monitoring GFP fluorescence,β-glucuronidase activity, or luminescence.

All publications and patent applications mentioned in this specificationare herein incorporated by reference to the same extent as if eachindividual publication or patent application was specifically andindividually indicated to be incorporated by reference.

The present invention is not limited by the specific embodimentsdescribed herein. The invention now being fully described, it will beapparent to one of ordinary skill in the art that many changes andmodifications can be made thereto without departing from the spirit orscope of the appended claims. Modifications that become apparent fromthe foregoing description and accompanying figures fall within the scopeof the claims.

What is claimed is:
 1. A recombinant polynucleotide having a firstpercent identity, and the recombinant polynucleotide encodes apolypeptide having a second percent identity to its full length or to aconserved domain comprised within the polypeptide; and thepolynucleotide is selected from the group consisting of SEQ ID NO: 1, 3,5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, 37, 39, 41,43, 45, 47, 49, 51, 53, 55, 57, 59, 61, 63, 65, 67, 69, 71, 73, 75, 77,79, 81, 83, 85, 87, 89, 91, 93, 95, 97, 99, 101, 103, 105, 107, 109,111, 113, 115, 117, 119, 121, 123, 125, 127, 129, 131, 133, 135, 137,139, 141, 143, 145, 147, 149, 151, 153, 155, 157, 159, 161, 163, 165,167, 169, 171, 173, 175, 177, 179, 181, 183, 185, 187, 189, 191, 193,195, 197, 199, 201, 203, 205, 207, 209, 211, 213, 215, 217, 219, 221,223, 225, 227, 229, 231, 233, 235, 237, 239, 241, 243, 245, 247, 249,251, 253, 255, 257, 259, 261, 263, 265, 267, 269, 271, 273, 275, 277,279, 281, 283, 285, 287, 289, 291, 293, 295, 297, 299, 301, 303, 305,307, 309, 311, 313, 315, 317, 319, 321, 323, 325, 327, 329, 331, 333,335, 337, 339, 341, 343, 345, 347, 349, 351, 353, 355, 357, 359, 361,363, 365, 367, 369, 371, 373, 375, 377, 379, 381, 383, 385, 387, 389,391, 393, 395, 397, 399, 401, 403, 405, 407, 409, 411, 413, 415, 417,419, 421, 423, 425, 427, 429, 431, 433, 435, 437, 439, 441, 443, 445,447, 449, 451, 453, 455, 457, 459, 461, 463, 465, 467, 469, 471, 473,475, 477, 479, 481, 483, 485, 487, 489, 491, 493, 495, 497, 499, 501,503, 505, 507, 509, 511, 513, 515, 517, 519, 521, 523, 525, 527, 529,531, 533, 535, 537, 539, 541, 543, 545, 547, 549, 551, 553, 555, 557,559, 561, 563, 565, 567, 569, 571, 573, 575, 577, 579, 581, 583, 585,587, 589, 591, 593, 595, 597, 599, 601, 603, 605, 607, 609, 611, 613,615, 617, 619, 621, 623, 625, 627, 629, 631, 633, 635, 637, 639, 641,643, 645, 647, 649, 651, 653, 655, 657, 659, 661, 663, 665, 667, 669,671, 673, 675, 677, 679, 681, 683, 685, 687, 689, 691, 693, 695, 697,699, 701, 703, 705, 707, 709, 711, 713, 715, 717, 719, 721, 723, 725,727, 729, 731, 733, 735, 737, 739, 741, 743, 745, 747, 749, 751, 753,755, 757, 759, 761, 763, 765, 767, 769, 771, 773, 775, 777, 779, 781,783, 785, 787, 789, 791, 793, 795, 797, 799, 801, 803, 805, 807, 809,811, 813, 815, 817, 819, 821, 823, 825, 827, 829, 831, 833, 835, 837,839, 841, 843, 845, 847, 849, 851, 853, 855, 857, 859, 861, 863, 865,867, 869, 871, 873, 875, 877, 879, 881, 883, 885, 887, 889, 891, 893,895, 897, 899, 901, 903, 905, 907, 909, 911, 913, 915, 917, 919, 921,923, 925, 927, 929, 931, 933, 935, 937, 939, 941, 943, 945, 947, 949,951, 953, 955, 957, 959, 961, 963, 965, 967, 969, 971, 973, 975, 977,979, 981, 983, 985, 987, 989, 991, 993, 995, 997, 999, 1001, 1003, 1005,1007, 1009, 1011, 1013, 1015, and 1017; or the polypeptide is selectedfrom the group consisting of SEQ ID NO: 2, 4, 6, 8, 10, 12, 14, 16, 18,20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48, 50, 52, 54,56, 58, 60, 62, 64, 66, 68, 70, 72, 74, 76, 78, 80, 82, 84, 86, 88, 90,92, 94, 96, 98, 100, 102, 104, 106, 108, 110, 112, 114, 116, 118, 120,122, 124, 126, 128, 130, 132, 134, 136, 138, 140, 142, 144, 146, 148,150, 152, 154, 156, 158, 160, 162, 164, 166, 168, 170, 172, 174, 176,178, 180, 182, 184, 186, 188, 190, 192, 194, 196, 198, 200, 202, 204,206, 208, 210, 212, 214, 216, 218, 220, 222, 224, 226, 228, 230, 232,234, 236, 238, 240, 242, 244, 246, 248, 250, 252, 254, 256, 258, 260,262, 264, 266, 268, 270, 272, 274, 276, 278, 280, 282, 284, 286, 288,290, 292, 294, 296, 298, 300, 302, 304, 306, 308, 310, 312, 314, 316,318, 320, 322, 324, 326, 328, 330, 332, 334, 336, 338, 340, 342, 344,346, 348, 350, 352, 354, 356, 358, 360, 362, 364, 366, 368, 370, 372,374, 376, 378, 380, 382, 384, 386, 388, 390, 392, 394, 396, 398, 400,402, 404, 406, 408, 410, 412, 414, 416, 418, 420, 422, 424, 426, 428,430, 432, 434, 436, 438, 440, 442, 444, 446, 448, 450, 452, 454, 456,458, 460, 462, 464, 466, 468, 470, 472, 474, 476, 478, 480, 482, 484,486, 488, 490, 492, 494, 496, 498, 500, 502, 504, 506, 508, 510, 512,514, 516, 518, 520, 522, 524, 526, 528, 530, 532, 534, 536, 538, 540,542, 544, 546, 548, 550, 552, 554, 556, 558, 560, 562, 564, 566, 568,570, 572, 574, 576, 578, 580, 582, 584, 586, 588, 590, 592, 594, 596,598, 600, 602, 604, 606, 608, 610, 612, 614, 616, 618, 620, 622, 624,626, 628, 630, 632, 634, 636, 638, 640, 642, 644, 646, 648, 650, 652,654, 656, 658, 660, 662, 664, 666, 668, 670, 672, 674, 676, 678, 680,682, 684, 686, 688, 690, 692, 694, 696, 698, 700, 702, 704, 706, 708,710, 712, 714, 716, 718, 720, 722, 724, 726, 728, 730, 732, 734, 736,738, 740, 742, 744, 746, 748, 750, 752, 754, 756, 758, 760, 762, 764,766, 768, 770, 772, 774, 776, 778, 780, 782, 784, 786, 788, 790, 792,794, 796, 798, 800, 802, 804, 806, 808, 810, 812, 814, 816, 818, 820,822, 824, 826, 828, 830, 832, 834, 836, 838, 840, 842, 844, 846, 848,850, 852, 854, 856, 858, 860, 862, 864, 866, 868, 870, 872, 874, 876,878, 880, 882, 884, 886, 888, 890, 892, 894, 896, 898, 900, 902, 904,906, 908, 910, 912, 914, 916, 918, 920, 922, 924, 926, 928, 930, 932,934, 936, 938, 940, 942, 944, 946, 948, 950, 952, 954, 956, 958, 960,962, 964, 966, 968, 970, 972, 974, 976, 978, 980, 982, 984, 986, 988,990, 992, 994, 996, 998, 1000, 1002, 1004, 1006, 1008, 1010, 1012, 1014,1016, 1018, 1019, 1020, 1021, 1022, 1023, 1024, 1025, 1026, 1027, 1028,1029, 1030, 1031, 1032, 1033, 1034, 1035, 1036, 1037, 1038, 1039, 1040,1041, 1042, 1043, 1044, 1045, 1046, 1047, 1048, 1049, 1050, 1051, 1052,1053, 1054, 1055, 1056, 1057, 1058, 1059, 1060, 1061, 1062, 1063, 1064,1065, 1066, 1067, 1068, 1069, 1070, 1071, 1072, 1073, 1074, 1075, 1076,1077, 1078, 1079, 1080, 1081, 1082, 1083, 1084, 1085, 1086, 1087, 1088,1089, 1090, 1091, 1092, 1093, 1094, 1095, 1096, 1097, 1098, 1099, 1100,1101, 1102, 1103, 1104, 1105, 1106, 1107, 1108, 1109, 1110, 1111, 1112,1113, 1114, 1115, 1116, 1117, 1118, 1119, 1120, 1121, 1122, 1123, 1124,1125, 1126, 1127, 1128, 1129, 1130, 1131, 1132, 1133, 1134, 1135, 1136,1137, 1138, 1139, 1140, 1141, 1142, 1143, 1144, 1145, 1146, 1147, 1148,1149, 1150, 1151, 1152, 1153, 1154, 1155, 1156, 1157, 1158, 1159, 1160,1161, 1162, 1163, 1164, 1165, 1166, 1167, 1168, 1169, 1170, 1171, 1172,1173, 1174, 1175, 1176, 1177, 1178, 1179, 1180, 1181, 1182, 1183, 1184,1185, 1186, 1187, 1188, 1189, 1190, 1191, 1192, 1193, 1194, 1195, 1196,1197, 1198, 1199, 1200, 1201, 1202, 1203, 1204, 1205, 1206, 1207, 1208,1209, 1210, 1211, 1212, 1213, 1214, 1215, 1216, 1217, 1218, 1219, 1220,1221, 1222, 1223, 1224, 1225, 1226, 1227, 1228, 1229, 1230, 1231, 1232,1233, 1234, 1235, 1236, 1237, 1238, 1239, 1240, 1241, 1242, 1243, 1244,1245, 1246, 1247, 1248, 1249, 1250, 1251, 1252, 1253, 1254, 1255, 1256,1257, 1258, 1259, 1260, 1261, 1262, 1263, 1264, 1265, 1266, 1267, 1268,1269, 1270, 1271, 1272, 1273, 1274, 1275, 1276, 1277, 1278, 1279, 1280,1281, 1282, 1283, 1284, 1285, 1286, 1287, 1288, 1289, 1290, 1291, 1292,1293, 1294, 1295, 1296, 1297, 1298, 1299, 1300, 1301, 1302, 1303, 1304,1305, 1306, 1307, 1308, 1309, 1310, 1311, 1312, 1313, 1314, 1315, 1316,1317, 1318, 1319, 1320, 1321, 1322, 1323, 1324, 1325, 1326, 1327, 1328,1329, 1330, 1331, 1332, 1333, 1334, 1335, 1336, 1337, 1338, 1339, 1340,1341, 1342, 1343, 1344, 1345, 1346, 1347, 1348, 1349, 1350, 1351, 1352,1353, 1354, 1355, 1356, 1357, 1358, 1359, 1360, 1361, 1362, 1363, 1364,1365, 1366, 1367, 1368, 1369, 1370, 1371, 1372, 1373, 1374, 1375, 1376,1377, 1378, 1379, 1380, 1381, 1382, 1383, 1384, 1385, 1386, 1387, 1388,1389, 1390, 1391, 1392, 1393, 1394, 1395, 1396, 1397, 1398, 1399, 1400,1401, 1402, 1403, 1404, 1405, 1406, 1407, 1408, 1409, 1410, 1411, 1412,1413, 1414, 1415, 1416, 1417, 1418, 1419, 1420, 1421, 1422, 1423, 1424,1425, 1426, 1427, 1428, 1429, 1430, 1431, 1432, 1433, 1434, 1435, and1436; and the first percent identity is selected from the groupconsisting of: at least 40%, at least 41%, at least 42%, at least 43%,at least 44%, at least 45%, at least 46%, at least 47%, at least 48%, atleast 49%, at least 50%, at least 51%, at least 52%, at least 53%, atleast 54%, at least 55%, at least 56%, at least 57%, at least 58%, atleast 59%, at least 60%, at least 61%, at least 62%, at least 63%, atleast 64%, at least 65%, at least 66%, at least 67%, at least 68%, atleast 69%, at least 70%, at least 71%, at least 72%, at least 73%, atleast 74%, at least 75%, at least 76%, at least 77%, at least 78%, atleast 79%, at least 80%, at least 81%, at least 82%, at least 83%, atleast 84%, at least 85%, at least 86%, at least 87%, at least 88%, atleast 89%, at least 90%, at least 91%, at least 92%, at least 93%, atleast 94%, at least 95%, at least 96%, at least 97%, at least 98%, atleast 99%, and about 100%; and the second percent identity is selectedfrom the group consisting of: at least 50%, at least 51%, at least 52%,at least 53%, at least 54%, at least 55%, at least 56%, at least 57%, atleast 58%, at least 59%, at least 60%, at least 61%, at least 62%, atleast 63%, at least 64%, at least 65%, at least 66%, at least 67%, atleast 68%, at least 69%, at least 70%, at least 71%, at least 72%, atleast 73%, at least 74%, at least 75%, at least 76%, at least 77%, atleast 78%, at least 79%, at least 80%, at least 81%, at least 82%, atleast 83%, at least 84%, at least 85%, at least 86%, at least 87%, atleast 88%, at least 89%, at least 90%, at least 91%, at least 92%, atleast 93%, at least 94%, at least 95%, at least 96%, at least 97%, atleast 98%, at least 99%, and about 100%.
 2. The recombinantpolynucleotide of claim 1, wherein when the recombinant polynucleotideis introduced into a plant and the polypeptide is ectopically expressedor overexpressed in the plant, the plant has an altered trait relativeto a control plant that does not ectopically express or overexpress therecombinant polynucleotide.
 3. The recombinant polynucleotide of claim2, wherein the altered trait is selected from the group consisting of:aerial rosettes; altered inflorescence development; alteredarchitecture; bushier plant; compact plant; altered branching; alteredc/n sensing; increased tolerance to nitrogen limitation; increasedgrowth on potassium-free medium; less anthocyanin; altered coloration;altered floral organ identity and development; altered flowerdevelopment; ectopic carpel tissue; altered flower structure; alteredflowering time; altered glucosinolate profile; altered inflorescencedevelopment; altered inflorescence structure; altered leaf development;altered leaf shape; altered leaf coloration; dark green color; shinyleaves; upwardly oriented leaves; increased tocopherol; increasedchlorophyll; increased carotenoids; longer hypocotyls and lack of apicalhook in response to ethylene; altered seed development, ripening,germination; altered seed fatty acid composition; altered seed oilcontent; reduction in 16:3 fatty acids; increased seed oil content;decreased seed oil content; increased seed protein content; decreasedseed protein content; increased total seed oil and protein content;altered seed shape; altered shoot development; altered structure ofvascular tissues; altered sugar sensing: greater tolerance to sucrose;more sensitive to glucose; more tolerant to glucose; reduced cotyledonexpansion in 5% glucose; altered tocopherol composition; reducedtrichome density; increased trichome density; increased trichome size;reduced trichome density; ectopic trichome formation; glabrous leaves;increased root hairs; increased tolerance to cold; increased toleranceto heat; reduced chlorosis in heat; increased tolerance to salt;increased tolerance to nacl and sucrose; increased tolerance to sucroseand glucose; increased tolerance to hyperosmotic stress; better rootgrowth in hyperosmotic stress; increased seedling vigor in the presenceof polyethylene glycol; better seedling vigor in hyperosmotic stress;better root growth in hyperosmotic stress; better seedling vigor in 150mm NaCl; better seedling vigor in 9.4% sucrose; decreased seedling vigoron high glucose; increased drought tolerance; constitutivephotomorphogenesis; decreased sensitivity to abscisic acid; insensitiveto aba; downward pedicels; early flowering; early senescence; lateflowering; ectopic trichome formation; increased trichome number; embryolethal; enlarged floral organs; short pedicels; enlarged seedlings;ethylene insensitive when germinated in the dark on acc; formation ofnecrotic lesions; leaf and hypocotyl necrosis; increased seedling vigorin cold; more freezing tolerant; homeotic transformations; increase in18:2 fatty acids; decrease in 18:3 fatty acids; increase inalpha-tocopherol; increase in chlorophyll a and b; increase in leafxylose; increase in M39480; increased anthocyanins; increased leaf fattyacids; increased leaf fatty acids; increased leaf wax; increased leafunsaturated fatty acids; increased lutein content; increased leaf size;faster development; increased plant size; increased seedling size;increased seed size; increased seed yield; increased resistance toBotrytis; increased resistance to Erysiphe; increased resistance toFusarium; increased susceptibility to Botrytis; increased susceptibilityto Erysiphe; increased susceptibility to Fusarium; increasedsusceptibility to Pseudomonas; increased resistance to Sclerotinia;increased susceptibility to Sclerotinia; increased resistance toglyphosate; increased tolerance to glyphosate; increased sensitivity toACC; increased shade tolerance; increased sensitivity to high peg;increased sensitivity to oxidative stress; long hypocotyls; longpetioles; reduced cell differentiation in meristem; more vascularbundles in stem; pale green leaves; loss of apical dominance; reducedapical dominance; reduced branching; reduced fertility; reduced lateralbranching; reduced lignin; reduced petals, sepals and stamens; reducedsize; short pedicels, downward pointing siliques; thicker stem; altereddistribution of vascular bundles; short stamen filaments; seed coloralteration; and smaller and more rounded seeds; increase inα-tocopherol; increased chlorophyll a; and increased chlorophyll b.
 4. Atransgenic plant transformed with the recombinant polynucleotide ofclaim
 1. 5. The transgenic plant of claim 4, wherein the recombinantpolynucleotide encodes a polypeptide the expression of which isregulated by a constitutive, an inducible, or a tissue-enhancedpromoter.
 6. A cultured host cell derived from the transgenic plant ofclaim 4, wherein the cultured host cell comprises the recombinantpolynucleotide.
 7. A transgenic seed produced from the transgenic plantof claim 4, wherein the transgenic seed comprises the recombinantpolynucleotide.
 8. A method for producing a transgenic plant having analtered trait, wherein the method comprises the steps of: (a) providinga recombinant polynucleotide of claim 1; (b) introducing the recombinantpolynucleotide into a plant; and (c) optionally, identifying an alteredtrait in the transgenic plant relative to a control plant that does notectopically express or overexpress the polypeptide; wherein the alteredtrait is relative to a control plant that does not ectopically expressor overexpress the recombinant polynucleotide.
 9. The method of claim 8,the method steps further comprising: (d) crossing the transgenic plantwith itself or another plant; and (e) selecting a transgenic seed thatdevelops as a result of said crossing; and (f) growing a progeny plantfrom the transgenic seed, thus producing a transgenic progeny planthaving increased the altered trait.